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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
Silk suture FDA UDI
Device Name
4-0 BLACK SILK SUTURE 18", C-17 NEEDLE 12MM, 3/8 CIRCLE REVERSE CUT FDA UDI
Model / Reference
PSN736S FDA UDI
Description
4-0 BLACK SILK SUTURE 18", C-17 NEEDLE 12MM, 3/8 CIRCLE REVERSE CUT FDA UDI

Identifiers

Catalog Number
PSN736S FDA UDI
Primary DI / UDI-DI
10889950001742 FDA UDI
FDA Product Code
GAP FDA UDI
GMDN Term
Silk suture FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5030 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: Silk suture

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 Silk suture.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f9423847-3f86-4fe2-8711-df0baeb3a7b7 36 fields · synced Jun 1, 2026