Emergency Oral Airways Kit

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name: Emergency Oral Airways Kit FDA UDI
Generic Name: Laryngoscope blade, single-use FDA UDI
Device Name: Emergency Oral Airways Kit Infant 40 mm, Child 60 mm, Small Adult 80 mm, Medium Adult 90 mm, Large Adult 100 mm, XL Adult 110 mm FDA UDI
Model / Reference: 4791 FDA UDI
Description: Emergency Oral Airways Kit Infant 40 mm, Child 60 mm, Small Adult 80 mm, Medium Adult 90 mm, Large Adult 100 mm, XL Adult 110 mm FDA UDI

Identifiers

Primary DI / UDI-DI: 00616784479118 FDA UDI
FDA Product Code: CAE FDA UDI
GMDN Term: Laryngoscope blade, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5110 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

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

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Laryngoscope blade, single-use

Emergency Oral Airways Kit by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Disposable Conventional Laryngoscope Blade — Maco International · 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: Dynarex Corp.

Sources (1)

FDA UDI 5932836e-aaad-4a47-b36a-a1cf017efb6e 33 fields · synced May 30, 2026