|
Date of Entry
|
Specialty Task Group Area
|
Recognition Number
|
Standards Developing Organization
|
Standard Designation Number and Date
|
Title of Standard |
12/23/2019 |
General Plastic Surgery/ General Hospital |
6-438 |
ANSI AAMI IEC |
80601-2-77:2020 |
Medical electrical equipment - Part 2-77: Particular requirements for the basic safety and essential performance of robotically assisted surgical equipment |
IEC |
80601-2-77 Edition 1.0 2019-07 |
Medical electrical equipment - Part 2-77: Particular requirements for the BASIC SAFETY and essential performance of ROBOTICALLY ASSISTED SURGICAL EQUIPMENT |
07/06/2020 |
General Plastic Surgery/ General Hospital |
6-439 |
ISO |
7886-2 Second edition 2020-04 |
Sterile hypodermic syringes for single use - Part 2: Syringes for use with power-driven syringe pumps |
07/06/2020 |
General Plastic Surgery/ General Hospital |
6-440 |
ASTM |
D3578-19 |
Standard Specification for Rubber Examination Gloves |
07/06/2020 |
General Plastic Surgery/ General Hospital |
6-441 |
ISO |
7886-3 Second edition 2020-05 |
Sterile hypodermic syringes for single use - Part 3: Auto-disabled syringes for fixed-dose immunization |
07/06/2020 |
General Plastic Surgery/ General Hospital |
6-442 |
ASTM |
D6977-19 |
Standard Specification for Polychloroprene Examination Gloves for Medical Application |
07/06/2020 |
General Plastic Surgery/ General Hospital |
6-443 |
ASTM |
D3577-19 |
Standard Specification for Rubber Surgical Gloves |
07/06/2020 |
General Plastic Surgery/ General Hospital |
6-444 |
ASTM |
D7103-19 |
Standard Guide for Assessment of Medical Gloves |
07/06/2020 |
General Plastic Surgery/ General Hospital |
6-445 |
ASTM |
D5250-19 |
Standard Specification for Poly(vinyl chloride) Gloves for Medical Application |
07/06/2020 |
General Plastic Surgery/ General Hospital |
6-446 |
ASTM |
D6319-19 |
Standard Specification for Nitrile Examination Gloves for Medical Application |
07/06/2020 |
General Plastic Surgery/ General Hospital |
6-447 |
ISO |
8536-4 Sixth edition 2019-09 |
Infusion equipment for medical use - Part 4: Infusion sets for single use, gravity feed |
12/21/2020 |
General Plastic Surgery/ General Hospital |
6-448 |
ASTM |
F2407-20 |
Standard Specification for Surgical Gowns Intended for Use in Healthcare Facilities |
12/21/2020 |
General Plastic Surgery/ General Hospital |
6-449 |
ASTM |
F1169-19 |
Standard Consumer Safety Specification for Full-Size Baby Cribs |
12/21/2020 |
General Plastic Surgery/ General Hospital |
6-450 |
IEC |
60601-2-50 Edition 3.0 2020-09 |
Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment |
03/01/2021 |
General Plastic Surgery/ General Hospital |
6-460 |
ASTM |
F3502-21 |
Standard Specification for Barrier Face Coverings |
06/07/2021 |
General Plastic Surgery/ General Hospital |
6-461 |
IEC |
60601-2-19 Edition 3.0 2020-09 |
Medical electrical equipment - Part 2-19: Particular requirements for the basic safety and essential performance of infant incubators |
06/07/2021 |
General Plastic Surgery/ General Hospital |
6-462 |
IEC |
60601-2-20 Edition 3.0 2020-09 |
Medical electrical equipment - Part 2-20: Particular requirements for the basic safety and essential performance of infant transport incubators |
06/07/2021 |
General Plastic Surgery/ General Hospital |
6-463 |
IEC |
60601-2-21 Edition 3.0 2020-09 |
Medical electrical equipment - Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmers |
12/20/2021 |
General Plastic Surgery/ General Hospital |
6-464 |
ISO |
11040-4 Third edition 2015-04-01 |
Prefilled syringes - Part 4: Glass barrels for injectables and sterilized subassembled syringes ready for filling [Including AMENDMENT 1 (2020)] |
12/20/2021 |
General Plastic Surgery/ General Hospital |
6-465 |
USP-NF |
M76090_03_01 |
Sodium Chloride Irrigation |
12/20/2021 |
General Plastic Surgery/ General Hospital |
6-466 |
USP-NF |
M76070_03_01 |
Sodium Chloride Injection |
12/20/2021 |
General Plastic Surgery/ General Hospital |
6-467 |
USP-NF |
M80200_04_01 |
Nonabsorbable Surgical Suture |
12/20/2021 |
General Plastic Surgery/ General Hospital |
6-468 |
USP-NF |
M99670_02_01 |
<881> Tensile Strength |
12/20/2021 |
General Plastic Surgery/ General Hospital |
6-469 |
USP-NF |
M99650_02_01 |
<861> Sutures - Diameter |
12/20/2021 |
General Plastic Surgery/ General Hospital |
6-470 |
USP-NF |
M99660_03_01 |
<871> Sutures - Needle Attachment |
12/20/2021 |
General Plastic Surgery/ General Hospital |
6-471 |
USP-NF |
M88880_05_01 |
Sterile Water for Irrigation |
12/20/2021 |
General Plastic Surgery/ General Hospital |
6-472 |
USP-NF |
M36660_04_01 |
Heparin Lock Flush Solution |
12/20/2021 |
General Plastic Surgery/ General Hospital |
6-473 |
USP-NF |
M80190_04_01 |
Absorbable Surgical Suture |
12/20/2021 |
General Plastic Surgery/ General Hospital |
6-474 |
ASTM |
F3352-19 |
Standard Specification for Isolation Gowns Intended for Use in Healthcare Facilities |
05/30/2022 |
General Plastic Surgery/ General Hospital |
6-475 |
ISO |
11608-4:2022 |
Needle-based injection systems for medical use - Requirements and test methods - Part 4: Needle-based injection systems containing electronics |
05/30/2022 |
General Plastic Surgery/ General Hospital |
6-476 |
ISO |
11608-2:2022 |
Needle-based injection systems for medical use - Requirements and test methods - Part 2: Double-ended pen needles |
05/30/2022 |
General Plastic Surgery/ General Hospital |
6-477 |
ISO |
11608-3:2022 |
Needle-based injection systems for medical use - Requirements and test methods - Part 3: Containers and integrated fluid paths |
05/30/2022 |
General Plastic Surgery/ General Hospital |
6-478 |
ISO |
11608-1:2022 |
Needle-based injection systems for medical use - Requirements and test methods - Part 1: Needle-based injection systems |
05/30/2022 |
General Plastic Surgery/ General Hospital |
6-479 |
ISO |
11608-5:2022 |
Needle-based injection systems for medical use - Requirements and test methods - Part 5: Automated functions |
05/30/2022 |
General Plastic Surgery/ General Hospital |
6-480 |
ISO |
11608-6:2022 |
Needle-based injection systems for medical use - Requirements and test methods - Part 6: On-body delivery |
05/30/2022 |
General Plastic Surgery/ General Hospital |
6-481 |
ANSI AAMI |
CN27:2021 |
General requirements for Luer activated valves (LAVs) incorporated into medical devices for intravascular applications |
05/30/2022 |
General Plastic Surgery/ General Hospital |
6-482 |
AAMI |
TIR101:2021 |
Fluid delivery performance testing for infusion pumps |
12/19/2022 |
General Plastic Surgery/ General Hospital |
6-483 |
IEC |
60601-2-35 Edition 2.0 2020-09 |
Medical electrical equipment - Part 2-35: Particular requirements for the basic safety and essential performance of heating devices using blankets, pads and mattresses and intended for heating in medical use |
12/19/2022 |
General Plastic Surgery/ General Hospital |
6-484 |
ASTM |
F3502-22a |
Standard Specification for Barrier Face Coverings |
12/19/2022 |
General Plastic Surgery/ General Hospital |
6-485 |
ISO |
7886-4 Second Edition 2018-11 |
Sterile hypodermic syringes for single use - Part 4: Syringes with re-use prevention feature |
09/09/2008 |
InVitro Diagnostics |
7-21 |
CLSI |
C42-A |
Erythrocyte Protoporphyrin Testing; Approved Guideline |
07/09/2014 |
InVitro Diagnostics |
7-48 |
CLSI |
C60-A |
Blood Alcohol Testing in the Clinical Laboratory; Approved Guideline |
03/18/2009 |
InVitro Diagnostics |
7-71 |
CLSI |
H15-A3 (Replaces H15-A2) |
Reference and Selected Procedures for the Quantitative Determination of Hemoglobin in Blood; Approved Standard - Third Edition |
08/20/2012 |
InVitro Diagnostics |
7-76 |
CLSI |
M15-A (Replaces M15-T) |
Laboratory Diagnosis of Blood-borne Parasitic Diseases; Approved Guideline |
03/08/2004 |
InVitro Diagnostics |
7-86 |
CLSI |
C29-A2 (Replaces C29-A) |
Standardization of Sodium and Potassium Ion Selective Electrode Systems to the Flame Photometric Reference Method; Approved Standard - Second Edition |
03/08/2004 |
InVitro Diagnostics |
7-87 |
CLSI |
C31-A2 (Replaces C31-A) |
Ionized Calcium Determinations: Precollection Variables, Specimen Choice, Collection, and Handling; Approved Guideline - Second Edition. |
03/08/2004 |
InVitro Diagnostics |
7-88 |
CLSI |
C37-A |
Preparation and Validation of Commutable Frozen Human Serum Pools as Secondary Reference Materials for Cholesterol Measurement Procedures; Approved Guideline |
03/08/2004 |
InVitro Diagnostics |
7-89 |
CLSI |
C39-A (Replaces C39-P) |
A Designated Comparison Method for the Measurement of Ionized Calcium in Serum; Approved Standard |
10/04/2004 |
InVitro Diagnostics |
7-104 |
CLSI |
H7-A3 |
Procedure for Determining Packed Cell Volume by the Microhematocrit Method - Second Edition; Approved Standard - Third Edition. |
10/04/2004 |
InVitro Diagnostics |
7-105 |
CLSI |
H30-A2 |
Procedure for the Determination of Fibrinogen in Plasma; Approved Guideline Second Edition |
11/08/2005 |
InVitro Diagnostics |
7-113 |
CLSI |
I/LA23-A (Replaces I/LA23-P) |
Assessing the Quality of Immunoassay Systems: Radioimmunoassays, and Enzyme, Fluorescence, and Luminescence Immunoassays; Approved Guideline |
09/09/2008 |
InVitro Diagnostics |
7-136 |
CLSI |
I/LA2-A2 (Replaces I/LA2-A) |
Quality Assurance of Laboratory Tests for Autoantibodies to Nuclear Antigens: (1) Indirect Flurescence Assay for Microscopy and (2) Microtiter Enzyme Immunoassay Methods; Approved Guideline - Second Edition. |
01/14/2019 |
InVitro Diagnostics |
7-139 |
CLSI |
QMS24, 3rd Edition September 2016 Replaces GP27-A2 and GP29-A2 |
Using Proficiency Testing to Improve the Clinical Laboratory; Approved Guideline - Second Edition |
03/18/2009 |
InVitro Diagnostics |
7-145 |
CLSI |
H42-A2 (Replaces H42-A) |
Enumeration of Immunologically Defined Cell Populations by Flow Cytometry; Approved Guideline - Second Edition. |
08/20/2012 |
InVitro Diagnostics |
7-148 |
CLSI |
M28-A2 (Replaces M28-A) |
Procedures for the Recovery and Identification of Parasites from the Intestinal Tract; Approved Guideline - Second Edition. |
03/16/2012 |
InVitro Diagnostics |
7-150 |
CLSI |
H43-A2 |
Clinical Flow Cytometry Analysis of Neoplastic Hematolymphoid Cells; Approved Guideline - Second Edition |
01/30/2014 |
InVitro Diagnostics |
7-152 |
CLSI |
EP12-A2 |
User Protocol for Evaluation of Qualitative Test Performance; Approved Guideline - Second Edition. |
09/09/2008 |
InVitro Diagnostics |
7-159 |
CLSI |
H21-A5 |
Collection, Transport, and Processing of Blood Specimens for Testing Plasma-Based Coagulation Assays and Molecular Hemostasis Assays |
09/09/2008 |
InVitro Diagnostics |
7-163 |
CLSI |
H56-A (Replaces H56-P) |
Body Fluid Analysis for Cellular Composition; Approved Guideline. |
03/16/2012 |
InVitro Diagnostics |
7-165 |
CLSI |
H20-A2 (Replaces H20-A) |
Reference Leukocyte (WBC) Differential Count (Proportional) and Evaluation of Instrumental Methods; Approved Standard - Second Edition |
03/16/2012 |
InVitro Diagnostics |
7-166 |
CLSI |
GP20-A2 (Replaces GP20-A) |
Fine Needle Aspiration Biopsy (FNAB) Techniques; Approved Guideline - Second Edition |
03/18/2009 |
InVitro Diagnostics |
7-170 |
CLSI |
I/LA21-A2 |
Clinical Evaluation of Immunoassays; Approved Guideline - Second Edition |
07/09/2014 |
InVitro Diagnostics |
7-175 |
CLSI |
C59-A |
Apoplipoprotein Immunoassays: Development and Recommended Performance Characteristics; Approved Guideline |
03/18/2009 |
InVitro Diagnostics |
7-176 |
CLSI |
I/LA30-A (Replaces I/LA30-P) |
Immunoassay Interference by Endogenous Antibodies; Approved Guideline. |
01/14/2019 |
InVitro Diagnostics |
7-178 |
CLSI |
M22-A3 Vol 24 No. 19 Replaces M22-A2 Vol. 16 No. 16 |
Quality Control for Commercially Prepared Microbiological Culture Media; Approved Standard - Third Edition |
03/18/2009 |
InVitro Diagnostics |
7-180 |
CLSI |
M34-A (Replaces M24-P) |
Western Blot Assay for Antibodies to Borrelia burgdorferi; Approved Guideline. |
03/18/2009 |
InVitro Diagnostics |
7-182 |
CLSI |
M36-A |
Clinical Use and Interpretation of Serologic Tests for Toxoplasma gondii; Approved Guideline. |
03/18/2009 |
InVitro Diagnostics |
7-185 |
CLSI |
M41-A |
Viral Culture; Approved Guideline. |
03/18/2009 |
InVitro Diagnostics |
7-189 |
CLSI |
M47-A (Replaces M47-P) |
Principles and Procedures for Blood Cultures; Approved Guideline |
03/18/2009 |
InVitro Diagnostics |
7-190 |
CLSI |
M50-A (Replaces M50-P) |
Quality Control for Commercial Microbial Identification Systems; Approved Guideline |
03/18/2009 |
InVitro Diagnostics |
7-192 |
CLSI |
MM18-A (Replaces MM18-P) |
Interpretive Criteria for Indentification of Bacteria and Fungi by DNA Target Sequencing; Approved Guideline |
08/20/2012 |
InVitro Diagnostics |
7-197 |
CLSI |
M35-A2 (Replaces M35-A) |
Abbreviated Identification of Bacteria and Yeast; Approved Guideline - Second Edition. |
05/05/2010 |
InVitro Diagnostics |
7-205 |
CLSI |
H47-A2 |
One-Stage Prothrombin Time (PT) Test and Activated Partial Thromboplastin Time (APTT) Test; Approved Guideline - Second Edition. |
05/05/2010 |
InVitro Diagnostics |
7-207 |
CLSI |
GP16-A3 (Replaces GP16-A2) |
Urinalysis; Approved Guideline - Third Edition |
01/30/2014 |
InVitro Diagnostics |
7-210 |
CLSI |
H26-A2 |
Validation, Verification, and Quality Assurance of Automated Hematology Analyzers; Proposed Standard - Second Edition |
10/04/2010 |
InVitro Diagnostics |
7-212 |
CLSI |
EP18-A2 |
Risk Management Techniques to Identify and Control Laboratory Error Sources; Approved Guideline - Second Edition |
07/09/2014 |
InVitro Diagnostics |
7-213 |
CLSI |
GP44-A4 (Formerly H18-A4) |
Procedures for the Handling and Processing of Blood Specimens for Common Laboratory Tests; Approved Guideline-Fourth Edition |
08/02/2011 |
InVitro Diagnostics |
7-219 |
CLSI |
I/LA28-A2 |
Quality Assurance for Design Control and Implementation of Immunohistochemistry Assays; Approved Guidelines-Second Edition. |
01/30/2014 |
InVitro Diagnostics |
7-220 |
CLSI |
H59-A (Replaces H59-P) |
Quantitative D-dimer for the Exclusion of Venous Thromboembolic Disease; Approved Guideline. |
07/09/2014 |
InVitro Diagnostics |
7-221 |
CLSI |
GP39-A6 (Formerly H01-A6) |
Tubes and Additives for Venous Blood Specimen Collection; Approved Standard-Sixth Edition |
01/30/2014 |
InVitro Diagnostics |
7-223 |
CLSI |
QMS06-A3 (Formerly GP22-A3) |
Quality Management System: Continual Improvement; Approved Guideline - Third Edition |
01/30/2014 |
InVitro Diagnostics |
7-224 |
CLSI |
EP28-A3c (Formerly C28-A3c) |
Defining, Establishing, and Verifying Reference Intervals in the Clinical Laboratory; Approved Guideline - Third Edition |
03/16/2012 |
InVitro Diagnostics |
7-225 |
CLSI |
GP34-A (Replaces GP34-P) |
Validation and Verfication of Tubes for Venous and Capillary Blood Specimen Collection; Approved Guidance |
03/16/2012 |
InVitro Diagnostics |
7-227 |
CLSI |
M53-A (Replaces M53-P) |
Criteria for Laboratory Testing and Diagnosis of Human Immunodeficiency Virus Infection; Approved Guideline |
01/14/2019 |
InVitro Diagnostics |
7-232 |
CLSI |
MM05-A2 Vol. 32 No. 6 Replaces MM05-A Vol. 23 No. 17 |
Nucleic Acid Amplification Assays for Molecular Hematopathology; Approved Guideline - Second Edition |
01/15/2013 |
InVitro Diagnostics |
7-233 |
CLSI |
EP17-A2 |
Evaluation of Detection Capability for Clinical Laboratory Measurement Procedures; Approved Guideline - Second Edition |
08/06/2013 |
InVitro Diagnostics |
7-234 |
CLSI |
EP24-A2 (Replaces GP 10-A) |
Assessment of the Diagnostic Accuracy of Laboratory Tests Using Receiver Operating Characteristic Curves; Approved Guideline - Second Edition |
01/15/2013 |
InVitro Diagnostics |
7-235 |
CLSI |
EP25-A (Replaces EP25-P) |
Evaluation of Stability of In Vitro Diagnostic Reagents; Approved Guideline. |
06/07/2021 |
InVitro Diagnostics |
7-236 |
CLSI |
M43-A October 2011 |
Methods for Antimicrobial Susceptibility Testing for Human Mycoplasmas; Approved Guideline |
01/15/2013 |
InVitro Diagnostics |
7-237 |
CLSI |
MM01-A3 (Replaces MM01-A2) |
Molecular Methods for Clinical Genetics and Oncology Testing; Approved Guideline - Third Edition |
01/15/2013 |
InVitro Diagnostics |
7-238 |
CLSI |
MM06-A2 (Replaces MM06-A) |
Quantitative Molecular Methods for Infectious Diseases; Approved Guideline - Second Edition |
01/30/2014 |
InVitro Diagnostics |
7-239 |
CLSI |
EP32-R (Formerly X05-R) |
Metrological Traceability and Its Implementation; A Report |
08/06/2013 |
InVitro Diagnostics |
7-242 |
CLSI |
C56-A |
Hemolysis, Icterus, and Lipemia/Turbidity Indices as Indicators of Interference in Clinical Laboratory Analysis; Approved Guideline |
08/06/2013 |
InVitro Diagnostics |
7-243 |
CLSI |
M51-A (Replaces M51-P) |
Method for Antifungal Disk Diffusion Susceptibility Testing of Nondermatophyte Filamentous Fungi; Approved Guideline |
01/30/2014 |
InVitro Diagnostics |
7-244 |
CLSI |
NBS01-A6 (Replaces LA04-A5) |
Blood Collection on Filter Paper for Newborn Screening Programs: Approved Standard - Sixth Edition |
01/27/2015 |
InVitro Diagnostics |
7-250 |
CLSI |
M40-A2 (Reaffirmed: September 2019) |
Quality Control of Microbiological Transport Systems; Approved Standard - Second Edition. |
08/14/2015 |
InVitro Diagnostics |
7-251 |
CLSI |
EP05-A3 (Reaffirmed: September 2019) |
Evaluation of Precision of Quantitative Measurement Procedures; Approved Guideline - Third Edition |
08/14/2015 |
InVitro Diagnostics |
7-252 |
CLSI |
EP14-A3 |
Evaluation of Commutability of Processed Samples; Approved Guideline - Third Edition |
08/14/2015 |
InVitro Diagnostics |
7-253 |
CLSI |
EP15-A3 (Reaffirmed: September 2019) |
User Verification of Precision and Estimation of Bias; Approved Guideline - Third Edition |
08/14/2015 |
InVitro Diagnostics |
7-255 |
CLSI |
MM09-A2 (Replaces MM09-A) |
Nucleic Acid Sequencing Methods in Diagnostic Laboratory Medicine: Approved Guideline -- Second Edition |
08/14/2015 |
InVitro Diagnostics |
7-257 |
CLSI |
M56-A |
Principles and procedures for Detection of Anaerobes in Clinical Specimens; Approved Guideline |