Hahnenkratt

FDA UDI

Class I (US FDA UDI)

by E. Hahnenkratt GmbH

Identity

Trade Name: Hahnenkratt FDA UDI
Generic Name: Laryngeal mirror, reusable FDA UDI
Device Name: without thread, Ø 24 mm FDA UDI
Model / Reference: H751RX24 FDA UDI
Description: without thread, Ø 24 mm FDA UDI

Identifiers

Primary DI / UDI-DI: E206H751RX240 FDA UDI
FDA Product Code: KAI FDA UDI
GMDN Term: Laryngeal mirror, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4420 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Laryngeal mirror, reusable

Hahnenkratt by E. Hahnenkratt GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Laryngeal mirror — Spiggle & Theis Medizintechnik GmbH · Class I
Laryngeal mirror, rhodium coated — Spiggle & Theis Medizintechnik GmbH · Class I
Marina Medical — MARINA MEDICAL INSTRUMENTS, INC. · Class I
LARYNGEAL MIRROR — SONTEC INSTRUMENTS, INC. · Class I
AESCULAP — AESCULAP, INC. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: E. Hahnenkratt GmbH

Sources (1)

FDA UDI dc68788a-f8f1-4e52-a138-718bb022b5fc 33 fields · synced Jun 1, 2026