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Medicon

FDA UDI

Class I (US FDA UDI)

by Medicon eG. Chirurgiemechaniker-Genossenschaft

Identity

Trade Name
Medicon FDA UDI
Generic Name
Laryngeal mirror, reusable FDA UDI
Device Name
laryng mirror 22cm fig 7 Ø 24mm FDA UDI
Model / Reference
73.48.24 FDA UDI
Description
laryng mirror 22cm fig 7 Ø 24mm FDA UDI

Identifiers

Catalog Number
73.48.24 FDA UDI
Primary DI / UDI-DI
04046826135072 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

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
Moist Heat or Steam Sterilization FDA UDI

Category: Laryngeal mirror, reusable

This laryng mirror is a reusable, hand-held manual surgical instrument designed for the accurate examination of the throat. Its long, slender shaft features a polished surface that reflects enough undiffused light to form a virtual image of an object placed before it at the distal end.

Similar devices

Also classified as Laryngeal mirror, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 95f38543-22e5-489a-9ddf-64a66f84a7b5 35 fields · synced Jun 21, 2026