Identity
- Trade Name
- DEKNATEL FDA UDI
- Generic Name
- Suture kit, non-medicated FDA UDI
- Device Name
- V-PAK(F6-7044GWM8)x2 FDA UDI
- Model / Reference
- IPN026620 FDA UDI
- Description
- V-PAK(F6-7044GWM8)x2 FDA UDI
Identifiers
- Catalog Number
- V-3789 FDA UDI
- Primary DI / UDI-DI
- 04026704555185 FDA UDI
- FDA Product Code
- OVN FDA UDI
- GMDN Term
- Suture kit, non-medicated 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
No
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Dimensions & Sizes
- Size
- Length — 36 Inch FDA UDI
Category: Suture kit, non-medicated
Deknatel by Teleflex Incorporated — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (1)
- FDA UDI 2fb2c12c-d442-4da8-bd6d-b5c627320697 36 fields · synced Jun 8, 2026