Identity
- Trade Name
- DEKNATEL FDA UDI
- Generic Name
- Cardiovascular patch, synthetic FDA UDI
- Device Name
- PLEDGET SOFT LARGE 6 INCHES X 6 INCHES FDA UDI
- Model / Reference
- IPN029169 FDA UDI
- Description
- PLEDGET SOFT LARGE 6 INCHES X 6 INCHES FDA UDI
Identifiers
- Catalog Number
- X-5468 FDA UDI
- Primary DI / UDI-DI
- 14026704646804 FDA UDI
- FDA Product Code
- DXZ FDA UDI
- GMDN Term
- Cardiovascular patch, synthetic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.3470 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
MR Safe FDA UDI
Dimensions & Sizes
- Size
- Length — 75 Centimeter FDA UDI
Category: Cardiovascular patch, synthetic
Deknatel by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cardiovascular patch, synthetic.
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- Bard® PTFE Felt — Bard Peripheral Vascular · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (1)
- FDA UDI 9b2667d3-47b2-46a9-b212-701868380c06 36 fields · synced May 30, 2026