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Michel Rhinoscopic Laryngeal Mirror

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Michel Rhinoscopic Laryngeal Mirror FDA UDI
Generic Name
Rhinoscopic mirror FDA UDI
Device Name
Michel Rhinoscopic Laryngeal Mirror 18 Millimeter Tip Size 3 FDA UDI
Model / Reference
502-203 FDA UDI
Description
Michel Rhinoscopic Laryngeal Mirror 18 Millimeter Tip Size 3 FDA UDI

Identifiers

Catalog Number
502-203 FDA UDI
Primary DI / UDI-DI
00192896097438 FDA UDI
FDA Product Code
KAI FDA UDI
GMDN Term
Rhinoscopic mirror 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
Dry Heat Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 11.5 Inch FDA UDI

Category: Rhinoscopic mirror

Michel Rhinoscopic Laryngeal Mirror by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rhinoscopic mirror.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sontec Instruments, Inc.

Sources (1)

  • FDA UDI 8e46d0a8-6c29-45d0-a001-b4b312a1b427 36 fields · synced Jun 1, 2026