Identity
- Trade Name
- DEKNATEL FDA UDI
- Generic Name
- Silk suture FDA UDI
- Device Name
- RC TIE SLK 4-0 18"X12 FDA UDI
- Model / Reference
- IPN025275 FDA UDI
- Description
- RC TIE SLK 4-0 18"X12 FDA UDI
Identifiers
- Catalog Number
- RC-1387 FDA UDI
- Primary DI / UDI-DI
- 14026704559678 FDA UDI
- FDA Product Code
- OVN FDA UDI
- GMDN Term
- Silk suture FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4830 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
Yes
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
Yes
FDA UDI
MR Safe FDA UDI
Dimensions & Sizes
- Size
- Length — 45 Centimeter FDA UDI
Category: Silk suture
Deknatel by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Silk suture.
- Sofsilk — Covidien LP · Class II
- PERMA-HAND — Ethicon Inc. · Class II
- DemeSILK — DemeTECH Corp · Class II
- DemeSILK — DemeTECH Corp · Class II
- DemeSILK — DemeTECH Corp · Class II
- Sofsilk — Covidien LP · Class II
- DemeSILK — DemeTECH Corp · Class II
- DemeSILK — DemeTECH Corp · 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 ab4f574b-0b01-4146-9774-363f073dad27 36 fields · synced May 30, 2026