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Sontec Freer Skin Hook

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Sontec Freer Skin Hook FDA UDI
Generic Name
Soft-tissue surgical hook, reusable FDA UDI
Device Name
Sontec Freer Skin Hook Flat Handle 2 Blunt Prongs Titanium FDA UDI
Model / Reference
199-401T FDA UDI
Description
Sontec Freer Skin Hook Flat Handle 2 Blunt Prongs Titanium FDA UDI

Identifiers

Catalog Number
199-413T FDA UDI
Primary DI / UDI-DI
00192896118157 FDA UDI
FDA Product Code
GDG FDA UDI
GMDN Term
Soft-tissue surgical hook, reusable 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

No

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Dry Heat Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 6 Inch FDA UDI

Category: Soft-tissue surgical hook, reusable

Sontec Freer Skin Hook by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Soft-tissue surgical hook, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 98feac63-c5ee-4ed0-9ed1-853f60719bbb 36 fields · synced Jun 8, 2026