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Hermann Medizintechnik GmbH

FDA UDI

Class I (US FDA UDI)

by Hermann Medizintechnik GmbH

Identity

Trade Name
Hermann Medizintechnik GmbH FDA UDI
Generic Name
Skin/tissue hook FDA UDI
Device Name
FREEMAN RAKE retractor 18 cm4 prongs, 38 mm wide FDA UDI
Model / Reference
H118-25238 FDA UDI
Description
FREEMAN RAKE retractor 18 cm4 prongs, 38 mm wide FDA UDI

Identifiers

Primary DI / UDI-DI
04059453019059 FDA UDI
FDA Product Code
EIG FDA UDI
GMDN Term
Skin/tissue hook FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

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

No

FDA UDI

Category: Skin/tissue hook

Hermann Medizintechnik GmbH by Hermann Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin/tissue hook.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a1affd9f-f24c-4d51-bd97-8449972dbfd7 34 fields · synced May 30, 2026