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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device ventilator, non-continuous (respirator)
Product CodeBZD
Regulation Number 868.5905
Device Class 2


Premarket Reviews
ManufacturerDecision
3B MEDICAL, INC.
  SUBSTANTIALLY EQUIVALENT 2
APEX MEDICAL CORP.
  SUBSTANTIALLY EQUIVALENT 2
BMC MEDICAL CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1
  1.  K211155  Auto CPAP System
FISHER & PAYKEL HEALTHCARE LTD
  SUBSTANTIALLY EQUIVALENT 3
FISHER & PAYKEL HEALTHCARE LTD.
  SUBSTANTIALLY EQUIVALENT 2
FISHER AND PAYKEL HEALTHCARE LIMITED
  SUBSTANTIALLY EQUIVALENT 1
PHILIPS RESPIRONICS
  SUBSTANTIALLY EQUIVALENT 1
REMSLEEP HOLDINGS
  SUBSTANTIALLY EQUIVALENT 1
RESMED CORP
  SUBSTANTIALLY EQUIVALENT 3
RESMED LTD
  SUBSTANTIALLY EQUIVALENT 1
RESMED PTY LTD
  SUBSTANTIALLY EQUIVALENT 1
RESMED PTY LTD (REGISTRATION NUMBER: 3004604967)
  SUBSTANTIALLY EQUIVALENT 3
RESPIRONICS INC.
  SUBSTANTIALLY EQUIVALENT 3
RESPIRONICS, INC.
  SUBSTANTIALLY EQUIVALENT 4
SLEEPNET CORPORATION
  SUBSTANTIALLY EQUIVALENT 5
SUZHOU YUYUE MEDICAL TECHNOLOGY CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1
SYSMED (CHINA) CO., LTD
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2019 188 188
2020 126 126
2021 6062 6062
2022 90783 90783
2023 27997 27997
2024 51901 51901

Device Problems MDRs with this Device Problem Events in those MDRs
Degraded 169483 169483
Contamination 3890 3890
Corroded 2461 2461
Adverse Event Without Identified Device or Use Problem 1084 1084
Nonstandard Device 759 759
Patient-Device Incompatibility 390 390
Device Emits Odor 369 369
Smoking 253 253
Insufficient Information 248 248
Material Integrity Problem 242 242
Overheating of Device 238 238
Fire 170 170
Noise, Audible 163 163
Excessive Heating 161 161
Patient Device Interaction Problem 149 149
Contamination /Decontamination Problem 129 129
Temperature Problem 116 116
Mechanical Problem 109 109
Particulates 108 108
Failure to Power Up 104 104
Device Contamination with Chemical or Other Material 101 101
No Apparent Adverse Event 100 100
Thermal Decomposition of Device 68 68
Break 62 62
Disconnection 57 57
Product Quality Problem 52 52
Defective Device 46 46
Unexpected Shutdown 44 44
Power Problem 43 43
Activation Problem 42 42
Pressure Problem 41 41
Obstruction of Flow 40 40
Circuit Failure 39 39
Peeled/Delaminated 37 37
Decrease in Pressure 35 35
Appropriate Term/Code Not Available 35 35
Complete Loss of Power 35 35
Sparking 34 34
Detachment of Device or Device Component 32 32
Use of Device Problem 32 32
Electrical /Electronic Property Problem 32 32
Increase in Pressure 30 30
Unraveled Material 30 30
Leak/Splash 29 29
Therapeutic or Diagnostic Output Failure 28 28
Output Problem 26 26
Melted 26 26
Material Disintegration 25 25
Crack 23 23
Insufficient Heating 23 23

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 98688 98688
Unspecified Respiratory Problem 26487 26487
Headache 21867 21867
Dizziness 14783 14783
Cancer 13502 13502
Dyspnea 12087 12087
Asthma 12001 12001
Respiratory Tract Infection 9585 9585
Sore Throat 8120 8120
Unspecified Kidney or Urinary Problem 7771 7771
Cough 7635 7635
Skin Inflammation/ Irritation 5440 5440
Nausea 5222 5222
Inflammation 4786 4786
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 3917 3917
Vomiting 3886 3886
Hypersensitivity/Allergic reaction 3630 3630
Unspecified Heart Problem 3413 3413
Unspecified Hepatic or Biliary Problem 2034 2034
Dry Mouth 1901 1901
Insufficient Information 1834 1834
Chronic Obstructive Pulmonary Disease (COPD) 1711 1711
Chest Pain 1529 1529
Pneumonia 1193 1193
Sleep Dysfunction 1164 1164
Epistaxis 1073 1073
Heart Failure/Congestive Heart Failure 1034 1034
Fatigue 984 984
Liver Damage/Dysfunction 966 966
Bronchitis 825 825
Nodule 811 811
Dry Eye(s) 598 598
Unspecified Eye / Vision Problem 546 546
Pain 539 539
Stroke/CVA 488 488
Pulmonary Dysfunction 485 485
Apnea 470 470
High Blood Pressure/ Hypertension 459 459
Respiratory Failure 453 453
Sneezing 432 432
Burning Sensation 374 374
Breast Cancer 365 365
Cardiovascular Insufficiency 345 345
Swelling/ Edema 345 345
Nasal Obstruction 331 331
Lymphoma 326 326
Choking 324 324
Rash 306 306
Wheezing 294 294
Anxiety 262 262

Recalls
Manufacturer Recall Class Date Posted
1 Draeger Medical, Inc. I May-17-2023
2 Galemed Corporation I Dec-20-2019
3 Philips Respironics, Inc. I Apr-06-2023
4 Philips Respironics, Inc. I Sep-30-2022
5 Philips Respironics, Inc. I Jul-13-2021
6 ResMed Ltd. I Dec-21-2023
7 SleepNet Corporation I Apr-01-2024
8 TELEFLEX-MORRISVILLE I Nov-07-2019
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