Reusable Laryngeal Airway Mask

FDA UDI

Class I (US FDA UDI)

by Besmed Health Business Corp.

Identity

Trade Name: REUSABLE LARYNGEAL AIRWAY MASK FDA UDI
Generic Name: Oropharyngeal airway, reusable FDA UDI
Device Name: REUSABLE LARYNGEAL AIRWAY MASK SIZE:2.5; AMBU Code:340250000 FDA UDI
Model / Reference: LA-77325 FDA UDI
Description: REUSABLE LARYNGEAL AIRWAY MASK SIZE:2.5; AMBU Code:340250000 FDA UDI

Identifiers

Primary DI / UDI-DI: 04716770773254 FDA UDI
FDA Product Code: CAE FDA UDI
GMDN Term: Oropharyngeal airway, reusable 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

Yes

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Oropharyngeal airway, reusable

Reusable Laryngeal Airway Mask by Besmed Health Business Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Besmed Health Business Corp.

Sources (1)

FDA UDI 05d25bfb-4cbf-4b53-afba-024b5987d2d2 33 fields · synced Jun 6, 2026