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Hu-Friedy Mfg. Co., LLC

FDA UDI

Class II (US FDA UDI)

by Hu-Friedy Mfg Co., Llc

Identity

Trade Name
Hu-Friedy Mfg. Co., LLC FDA UDI
Generic Name
Polyester suture, non-bioabsorbable, multifilament FDA UDI
Device Name
4-0 GREEN POLYESTER SUTURE 18", C-6 NEEDLE 18.7MM, 3/8 CIRCLE REVERSE CUT FDA UDI
Model / Reference
PSNR683L FDA UDI
Description
4-0 GREEN POLYESTER SUTURE 18", C-6 NEEDLE 18.7MM, 3/8 CIRCLE REVERSE CUT FDA UDI

Identifiers

Catalog Number
PSNR683L FDA UDI
Primary DI / UDI-DI
10889950002060 FDA UDI
FDA Product Code
GAO FDA UDI
GMDN Term
Polyester suture, non-bioabsorbable, multifilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4495 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

Category: Polyester suture, non-bioabsorbable, multifilament

Hu-Friedy Mfg. Co., LLC by Hu-Friedy Mfg Co., Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyester suture, non-bioabsorbable, multifilament.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hu-Friedy Mfg Co., Llc

Sources (1)

  • FDA UDI f74e2e30-da01-4c97-810b-c6df4d71b257 36 fields · synced May 31, 2026