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Laryngeal Mirror

FDA UDI

Class I (US FDA UDI)

by Dr.frigz International(pvt)ltd,

Identity

Trade Name
LARYNGEAL MIRROR FDA UDI
Generic Name
Laryngeal mirror, single-use FDA UDI
Device Name
LARYNGEAL MIRROR NO-3, 8" FINISH FDA UDI
Model / Reference
LARYNGEAL MIRROR FDA UDI
Description
LARYNGEAL MIRROR NO-3, 8" FINISH FDA UDI

Identifiers

Catalog Number
LYM3 FDA UDI
Primary DI / UDI-DI
B974LYM30 FDA UDI
FDA Product Code
KAI FDA UDI
GMDN Term
Laryngeal mirror, single-use 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

Yes

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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 8 Inch FDA UDI

Category: Laryngeal mirror, single-use

Laryngeal Mirror by Dr.frigz International(pvt)ltd, — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngeal mirror, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dr.frigz International(pvt)ltd,

Sources (1)

  • FDA UDI 6b28ae4d-3d29-4488-8e66-a682fcff3493 35 fields · synced May 30, 2026