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Emta

FDA UDI

Class II (US FDA UDI)

by Foremount Enterprise Co., Ltd.

Identity

Trade Name
Emta FDA UDI
Generic Name
Resuscitator face mask, single-use FDA UDI
Device Name
Adult/Child CPR Mask in White Hard Case FDA UDI
Model / Reference
ME6201-FAK5000G-EMTA FDA UDI
Description
Adult/Child CPR Mask in White Hard Case FDA UDI

Identifiers

Primary DI / UDI-DI
04719871891599 FDA UDI
FDA Product Code
CBP FDA UDI
GMDN Term
Resuscitator face mask, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5870 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Resuscitator face mask, single-use

Emta by Foremount Enterprise Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Resuscitator face mask, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c883bd8d-5978-48ad-a39c-91351efbe5e0 33 fields · synced May 31, 2026