Identity
- Trade Name
- DEKNATEL FDA UDI
- Generic Name
- Suture kit, non-medicated FDA UDI
- Device Name
- V-PAK (X-5460GWM10) X1 FDA UDI
- Model / Reference
- IPN026568 FDA UDI
- Description
- V-PAK (X-5460GWM10) X1 FDA UDI
Identifiers
- Catalog Number
- V-3727A FDA UDI
- Primary DI / UDI-DI
- 04026704554966 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 — 30 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 dceb0046-ab6e-47da-a7b0-7ccfa571f84f 36 fields · synced May 30, 2026