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AuraGain

FDA UDI

Class I (US FDA UDI)

by Ambu A/S

Identity

Trade Name
AuraGain FDA UDI
Generic Name
Laryngeal mask airway, single-use FDA UDI
Device Name
Ambu AuraGain Size 1 FDA UDI
Model / Reference
408100000 FDA UDI
Description
Ambu AuraGain Size 1 FDA UDI

Identifiers

Catalog Number
408100000 FDA UDI
Primary DI / UDI-DI
05707480132058 FDA UDI
FDA Product Code
CAE FDA UDI
GMDN Term
Laryngeal mask airway, 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Laryngeal mask airway, single-use

AuraGain by Ambu A/S — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngeal mask airway, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ambu A/S

Sources (1)

  • FDA UDI 6d614c6b-27b8-4924-8b86-2a13024dd588 36 fields · synced May 31, 2026