Identity
- Trade Name
- TAUT FDA UDI
- Generic Name
- Peritoneal drainage catheter FDA UDI
- Device Name
- TAUT INTRADUCERS 10/BOX 7.5 FRENCH X 3.5 FDA UDI
- Model / Reference
- IPN927863 FDA UDI
- Description
- TAUT INTRADUCERS 10/BOX 7.5 FRENCH X 3.5 FDA UDI
Identifiers
- Catalog Number
- PI-93 FDA UDI
- Primary DI / UDI-DI
- 14026704912824 FDA UDI
- FDA Product Code
- GBW FDA UDI
- GMDN Term
- Peritoneal 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
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 6 Inch FDA UDIWidth — 2 Inch FDA UDIDepth — 0.5 Inch FDA UDI
Category: Peritoneal drainage catheter
Taut by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Peritoneal drainage catheter.
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- ACCEL™ — B BRAUN INTERVENTIONAL SYSTEMS, INC · Class I
- ACCEL™ — B BRAUN INTERVENTIONAL SYSTEMS, 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
- Teleflex Incorporated
Sources (1)
- FDA UDI db3cbdc0-706c-4bf0-a461-09ce79fb4efd 36 fields · synced May 30, 2026