← Back to catalogue

Top Safety

FDA UDI

Class II (US FDA UDI)

by Foremount Enterprise Co., Ltd.

Identity

Trade Name
Top Safety FDA UDI
Generic Name
Resuscitator face mask, single-use FDA UDI
Device Name
Pocket Mask Combo Pack- Zip Bag FDA UDI
Model / Reference
05-605-555C2B FDA UDI
Description
Pocket Mask Combo Pack- Zip Bag FDA UDI

Identifiers

Primary DI / UDI-DI
04719871891001 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Resuscitator face mask, single-use

Top Safety 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 39874a5c-d9eb-4e48-ac35-63179c394368 33 fields · synced May 30, 2026