Identity
- Trade Name
- DRIVEMEDICAL FDA UDI
- Generic Name
- Inspiratory/expiratory limb respiratory tubing, reusable FDA UDI
- Device Name
- RespiratoryRespiratory Disposables Product Description: Water trap.O2 Conc.50/cs FDA UDI
- Model / Reference
- CON 900 FDA UDI
- Description
- RespiratoryRespiratory Disposables Product Description: Water trap.O2 Conc.50/cs FDA UDI
Identifiers
- Primary DI / UDI-DI
- 50822383127229 FDA UDI
- FDA Product Code
- BYH FDA UDI
- GMDN Term
- Inspiratory/expiratory limb respiratory tubing, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5995 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Inspiratory/expiratory limb respiratory tubing, reusable
Drivemedical by Drive Devilbiss Healthcare — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- CPAP Tubing — SUNSET HEALTHCARE SOLUTIONS, Inc. · Class I
- CPAP Tubing — SUNSET HEALTHCARE SOLUTIONS, Inc. · Class I
- CPAP Kit — SUNSET HEALTHCARE SOLUTIONS, Inc.
- CPAP Tubing — SUNSET HEALTHCARE SOLUTIONS, Inc. · Class I
- Fisher & Paykel Healthcare — FISHER & PAYKEL HEALTHCARE, INC. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Drive Devilbiss Healthcare
Sources (1)
- FDA UDI f1ea069c-2d8e-4634-8167-537804667cf5 33 fields · synced Jun 8, 2026