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King Mask

FDA UDI

Class I (US FDA UDI)

by Ambu A/S

Identity

Trade Name
King Mask FDA UDI
Generic Name
Anaesthesia face mask, single-use FDA UDI
Device Name
Cherry scented disposable anesthesia face mask FDA UDI
Model / Reference
1345 FDA UDI
Description
Cherry scented disposable anesthesia face mask FDA UDI

Identifiers

Catalog Number
1345 FDA UDI
Primary DI / UDI-DI
00612649185163 FDA UDI
FDA Product Code
BSJ FDA UDI
GMDN Term
Anaesthesia face mask, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5550 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

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: Anaesthesia face mask, single-use

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

Similar devices

Also classified as Anaesthesia face mask, 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 7f2ca6bd-e8da-454d-824b-206e91b06789 37 fields · synced May 30, 2026