Identity
- Trade Name
- SUPRAMID FDA UDI
- Generic Name
- Nylon suture, non-bioabsorbable, monofilament FDA UDI
- Device Name
- 1/4 Circle Spatulated Double-Arm Needle (8mm), USP 5-0 SUPRAMID white monofilament Nylon, 12" FDA UDI
- Model / Reference
- 2S-1-50 FDA UDI
- Description
- 1/4 Circle Spatulated Double-Arm Needle (8mm), USP 5-0 SUPRAMID white monofilament Nylon, 12" FDA UDI
Identifiers
- Catalog Number
- 2S-1-50W FDA UDI
- Primary DI / UDI-DI
- 10816848020229 FDA UDI
- FDA Product Code
- GAR FDA UDI
- GMDN Term
- Nylon suture, non-bioabsorbable, monofilament FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.5020 FDA UDI
- Commercial Distribution
- Not 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
Supramid by S. Jackson, Inc. — 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
- S. Jackson, Inc.
Sources (1)
- FDA UDI 185cfefe-fde5-425a-b5ef-e2a082197669 35 fields · synced May 29, 2026