Identity
- Trade Name
- TAUT FDA UDI
- Generic Name
- Multi-purpose percutaneous abdominothoracic drainage catheter FDA UDI
- Device Name
- TAUT CHOLANGIOGRAPHY CATHETER 10/BOX 6.5 FRENCH X 18 INCHES FDA UDI
- Model / Reference
- IPN925154 FDA UDI
- Description
- TAUT CHOLANGIOGRAPHY CATHETER 10/BOX 6.5 FRENCH X 18 INCHES FDA UDI
Identifiers
- Catalog Number
- 965700 FDA UDI
- Primary DI / UDI-DI
- 14026704742513 FDA UDI
- FDA Product Code
- GBZ FDA UDI
- GMDN Term
- Multi-purpose percutaneous abdominothoracic drainage catheter FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4200 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
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
- Length — 18 Inch FDA UDIWidth — 2.2 Millimeter FDA UDI
Category: Multi-purpose percutaneous abdominothoracic drainage catheter
Taut by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Teleflex Incorporated
Sources (1)
- FDA UDI caa423d1-a50b-4e9d-bf0a-74ad1b2d2462 36 fields · synced May 30, 2026