Identity
- Trade Name
- ORTHOCORD FDA UDI
- Generic Name
- Polyester suture, bioabsorbable, monofilament, non-antimicrobial FDA UDI
- Device Name
- ORTHOCORD Violet Braided Composite Suture BB 17 mm 3/8c, Taper Point N=1 Meets U.S.P. and E.P. except for diameter 3-0 (2 metric), 18 Inches (45 cm) FDA UDI
- Model / Reference
- 223125 FDA UDI
- Description
- ORTHOCORD Violet Braided Composite Suture BB 17 mm 3/8c, Taper Point N=1 Meets U.S.P. and E.P. except for diameter 3-0 (2 metric), 18 Inches (45 cm) FDA UDI
Identifiers
- Catalog Number
- 223125 FDA UDI
- Primary DI / UDI-DI
- 10886705022939 FDA UDI
- 510(k) Number
- K123668 FDA UDI
- FDA Product Code
- GAT FDA UDINEW FDA UDI
- GMDN Term
- Polyester suture, bioabsorbable, monofilament, non-antimicrobial FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.5000 FDA UDI878.4840 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
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
Category: Polyester suture, bioabsorbable, monofilament, non-antimicrobial
Orthocord by Medos International Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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
- Medos International Sàrl
Sources (1)
- FDA UDI 0c40f259-3cfa-4bb4-a81f-b86a4cc2c077 36 fields · synced Jun 8, 2026