Identity
- Trade Name
- Syneture FDA UDI
- Generic Name
- Suture kit, non-medicated FDA UDI
- Device Name
- Custom Suture Pack, (1) 8886312551, (2) 8886316751, (1) 8886319151, (2) CL811, (1) CL915, (2) CN792, (1) S199, (1) S304, (1) VP521X, (1) VP733X, (2) VP772X, (1) VPF735X, (4) VS845 FDA UDI
- Model / Reference
- US1747 FDA UDI
- Description
- Custom Suture Pack, (1) 8886312551, (2) 8886316751, (1) 8886319151, (2) CL811, (1) CL915, (2) CN792, (1) S199, (1) S304, (1) VP521X, (1) VP733X, (2) VP772X, (1) VPF735X, (4) VS845 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10884521782679 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
- Not 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
Syneture by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 dd9472d8-775a-4e0e-ae3b-867c4f69a3de 36 fields · synced Jun 1, 2026