Identity
- Trade Name
- Syneture FDA UDI
- Generic Name
- Suture kit, medicated FDA UDI
- Device Name
- Custom Suture Pack, (1) CC-922, (2) CL-905, (1) CL-925, (1) CL-953, (2) GLS-322, (2) GS-62-M, (2) S-183, (1) S-184, (1) S-185, (2) S-187, (2) SL-5640, (1) VP-557-X, (3) VP-558-X, (2) VP-725-X, (1) VP-726-X, (1) VPF-522-X FDA UDI
- Model / Reference
- US1688 FDA UDI
- Description
- Custom Suture Pack, (1) CC-922, (2) CL-905, (1) CL-925, (1) CL-953, (2) GLS-322, (2) GS-62-M, (2) S-183, (1) S-184, (1) S-185, (2) S-187, (2) SL-5640, (1) VP-557-X, (3) VP-558-X, (2) VP-725-X, (1) VP-726-X, (1) VPF-522-X FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10884521512818 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
- 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 3799fb4e-a229-4364-974d-b98748a81def 36 fields · synced Jun 8, 2026