Identity
- Trade Name
- Syneture FDA UDI
- Generic Name
- Suture kit, medicated FDA UDI
- Device Name
- Custom Suture Pack,(2) 88862615-53;(2) CL-924;(2) CS-482;(2) GL-122;(1) GS-832;(2) GS-834;(1) S-183;(1) S-184;(1) SN-627;(2) VPF-713-X;(2) VS-845 FDA UDI
- Model / Reference
- US0840A FDA UDI
- Description
- Custom Suture Pack,(2) 88862615-53;(2) CL-924;(2) CS-482;(2) GL-122;(1) GS-832;(2) GS-834;(1) S-183;(1) S-184;(1) SN-627;(2) VPF-713-X;(2) VS-845 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10884521159259 FDA UDI
- FDA Product Code
- OVN FDA UDI
- GMDN Term
- Suture kit, 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
Category: Suture kit, medicated
Syneture by Covidien LP — 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
- Covidien LP
Sources (1)
- FDA UDI aa0f9393-a995-4d16-887e-2ed42ded03e8 35 fields · synced Jun 8, 2026