Identity
- Trade Name
- Hu-Friedy Mfg. Co., LLC FDA UDI
- Generic Name
- Polyester suture, bioabsorbable, multifilament, non-antimicrobial FDA UDI
- Device Name
- 5-0 UNDYED PGAFA SUTURE 18", C-1 NEEDLE 10.7 MM, 3/8 CIRCLE PREMIUM REVERSE CUT FDA UDI
- Model / Reference
- PSN505FA FDA UDI
- Description
- 5-0 UNDYED PGAFA SUTURE 18", C-1 NEEDLE 10.7 MM, 3/8 CIRCLE PREMIUM REVERSE CUT FDA UDI
Identifiers
- Catalog Number
- PSN505FA FDA UDI
- Primary DI / UDI-DI
- 10889950001391 FDA UDI
- FDA Product Code
- GAM FDA UDI
- GMDN Term
- Polyester suture, bioabsorbable, multifilament, non-antimicrobial FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4493 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
Hu-Friedy Mfg. Co., LLC by Hu-Friedy Mfg Co., Llc — 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
- Hu-Friedy Mfg Co., Llc
Sources (1)
- FDA UDI 59395b78-4b2b-4e8b-93f4-05007fd62650 37 fields · synced May 30, 2026