Identity
- Trade Name
- Deaver T-Tube FDA UDI
- Generic Name
- Biliary drain FDA UDI
- Device Name
- Deaver T-Tube, X-Ray Opaque Rubber, 12 Fr, FDA UDI
- Model / Reference
- 0099810 FDA UDI
- Description
- Deaver T-Tube, X-Ray Opaque Rubber, 12 Fr, FDA UDI
Identifiers
- Catalog Number
- 0099810 FDA UDI
- Primary DI / UDI-DI
- 00801741050343 FDA UDI
- FDA Product Code
- GBX FDA UDI
- GMDN Term
- Biliary drain FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4200 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
Yes
FDA UDI
Prescription Use
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Catheter Gauge — 12 French FDA UDI
Deaver T-Tube by C. R. Bard, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- C. R. Bard, Inc.
Sources (1)
- FDA UDI 70087ad6-7592-4fab-9516-be434ec11307 38 fields · synced Jun 1, 2026