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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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New Search show TPLC since Back to Search Results
Device analyzer, gas, carbon-dioxide, gaseous-phase
Product CodeCCK
Regulation Number 868.1400
Device Class 2


Premarket Reviews
ManufacturerDecision
BEIJING KINGST COMMERCIAL & TRADE CO.,LTD.
  SUBSTANTIALLY EQUIVALENT 2
BLUEPOINT MEDICAL GMBH & CO. KG
  SUBSTANTIALLY EQUIVALENT 1
CMI HEALTH INC.
  SUBSTANTIALLY EQUIVALENT 1
COVIDIEN
  SUBSTANTIALLY EQUIVALENT 1
COVIDIEN LLC
  SUBSTANTIALLY EQUIVALENT 2
DRAEGERWERK AG & CO. KGAA
  SUBSTANTIALLY EQUIVALENT 1
ENDURE INDUSTRIES INC
  SUBSTANTIALLY EQUIVALENT 1
ENGINEERED MEDICAL SYSTEMS INC.
  SUBSTANTIALLY EQUIVALENT 1
GE HEALTHCARE FINLAND OY
  SUBSTANTIALLY EQUIVALENT 3
MASIMO CORPORATION
  SUBSTANTIALLY EQUIVALENT 1
MAXTEC, LLC
  SUBSTANTIALLY EQUIVALENT 1
  1.  K182362  MaxCap Ped and MaxCap Neo
MEDIPINES CORPORATION
  SUBSTANTIALLY EQUIVALENT 1
MEDITERA TIBBI MALZEME SAN. VE TIC. A.S.
  SUBSTANTIALLY EQUIVALENT 1
NIHON KOHDEN CORPORATION
  SUBSTANTIALLY EQUIVALENT 2
ORANTECH INC.
  SUBSTANTIALLY EQUIVALENT 1
ORIDION MEDICAL 1987 LTD.
  SUBSTANTIALLY EQUIVALENT 3
PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH
  SUBSTANTIALLY EQUIVALENT 1
PNEUMA THERAPEUTICS, INC.
  SUBSTANTIALLY EQUIVALENT 1
POM MEDICAL, LLC
  SUBSTANTIALLY EQUIVALENT 1
RESPIRION, INC.
  SUBSTANTIALLY EQUIVALENT 1
REVOLUTIONARY MEDICAL DEVICES, INC.
  SUBSTANTIALLY EQUIVALENT 1
SOUTHMEDIC INC.
  SUBSTANTIALLY EQUIVALENT 1
TYLENOL MEDICAL INSTRUMENTS CO., LTD
  SUBSTANTIALLY EQUIVALENT 1
UNIMED MEDICAL SUPPLIES, INC.
  SUBSTANTIALLY EQUIVALENT 1
VENTURE THERAPEUTICS, INC.
  SUBSTANTIALLY EQUIVALENT 1
VYAIRE MEDICAL, INC.
  SUBSTANTIALLY EQUIVALENT 2

MDR Year MDR Reports MDR Events
2017 58 58
2018 63 63
2019 141 141
2020 2302 2302
2021 2272 2272
2022 2475 2475
2023 1638 1638
2024 948 948

Device Problems MDRs with this Device Problem Events in those MDRs
Break 3330 3330
Communication or Transmission Problem 2518 2518
Crack 2316 2316
Corroded 951 951
Appropriate Term/Code Not Available 944 944
Failure to Calibrate 880 880
Incorrect, Inadequate or Imprecise Result or Readings 737 737
Device Alarm System 620 620
Computer Software Problem 564 564
Contamination 522 522
Failure of Device to Self-Test 475 475
No Device Output 466 466
No Apparent Adverse Event 412 412
Loose or Intermittent Connection 408 408
Calibration Problem 375 375
Circuit Failure 300 300
Insufficient Information 295 295
Output Problem 220 220
Device Sensing Problem 184 184
Physical Resistance/Sticking 118 118
Failure to Read Input Signal 109 109
Display Difficult to Read 77 77
Display or Visual Feedback Problem 74 74
Application Program Freezes, Becomes Nonfunctional 62 62
Unable to Obtain Readings 58 58
Incorrect Measurement 50 50
Misassembled 49 49
Failure to Power Up 39 39
Peeled/Delaminated 38 38
Pumping Stopped 37 37
High Readings 35 35
Low Readings 34 34
Missing Information 31 31
Degraded 28 28
Naturally Worn 28 28
Application Program Problem 26 26
Failure to Cycle 25 25
Electrical /Electronic Property Problem 24 24
Power Problem 22 22
Temperature Problem 21 21
Gas Output Problem 20 20
Image Display Error/Artifact 19 19
Mechanical Problem 19 19
No Display/Image 17 17
Device Operates Differently Than Expected 16 16
Device Markings/Labelling Problem 15 15
Erratic or Intermittent Display 14 14
Device Displays Incorrect Message 13 13
Unexpected Shutdown 13 13
Noise, Audible 13 13

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 6613 6613
No Patient Involvement 3000 3000
No Known Impact Or Consequence To Patient 146 146
No Consequences Or Impact To Patient 143 143
Insufficient Information 121 121
No Information 88 88
Unintended Extubation 13 13
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 7 7
Unspecified Tissue Injury 4 4
Low Oxygen Saturation 4 4
Cardiac Arrest 3 3
Foreign Body In Patient 3 3
Hypoxia 3 3
Death 2 2
Respiratory Distress 2 2
Cyanosis 1 1
Superficial (First Degree) Burn 1 1
Patient Problem/Medical Problem 1 1
Hypersensitivity/Allergic reaction 1 1
Hypoventilation 1 1
Respiratory Arrest 1 1
Perforation 1 1
Burn, Thermal 1 1
Injury 1 1
Chest Pain 1 1
Discomfort 1 1
Cardiopulmonary Arrest 1 1
Laceration(s) 1 1
Pain 1 1
Anxiety 1 1
Cough 1 1
Partial thickness (Second Degree) Burn 1 1
Pressure Sores 1 1
Inadequate Pain Relief 1 1
Extubate 1 1
Respiratory Insufficiency 1 1
Death, Intrauterine Fetal 1 1
Lethargy 1 1

Recalls
Manufacturer Recall Class Date Posted
1 CareFusion 303, Inc. II Aug-30-2019
2 Covidien Llc II Dec-01-2020
3 GE Healthcare, LLC I Jan-10-2020
4 Nihon Kohden America Inc II Nov-06-2024
5 Oridion Medical 1987 Ltd. II Oct-03-2018
6 Smiths Medical ASD Inc. II Jul-06-2018
7 Southmedic, Inc. II Jul-24-2021
8 Southmedic, Inc. II Jan-25-2018
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