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Hook

FDA UDI

Class I (US FDA UDI)

by Dr.frigz International(pvt)ltd,

Identity

Trade Name
HOOK FDA UDI
Generic Name
Soft-tissue surgical hook, single-use FDA UDI
Device Name
SKIN HOOK, 1 PRONG BLUNT 6-1/2" FDA UDI
Model / Reference
SKIN HOOK FDA UDI
Description
SKIN HOOK, 1 PRONG BLUNT 6-1/2" FDA UDI

Identifiers

Catalog Number
25762 FDA UDI
Primary DI / UDI-DI
B9742576208 FDA UDI
FDA Product Code
GDG FDA UDI
GMDN Term
Soft-tissue surgical hook, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 6.5 Inch FDA UDI

Category: Soft-tissue surgical hook, single-use

Hook by Dr.frigz International(pvt)ltd, — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Soft-tissue surgical hook, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d580cde6-8c38-4395-90e6-841a9e808bd8 35 fields · synced Jun 8, 2026