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The Sea

FDA UDI

Class II (US FDA UDI)

by Mexpo International, Inc.

Identity

Trade Name
THE SEA FDA UDI
Generic Name
Surgical/medical face mask, non-antimicrobial, single-use FDA UDI
Device Name
3 PLY BACTERIAL FILTER FACE MASK ELASTIC EARLOOP- JELLY FISH (BLUE) FDA UDI
Model / Reference
TS FM-B24141 FDA UDI
Description
3 PLY BACTERIAL FILTER FACE MASK ELASTIC EARLOOP- JELLY FISH (BLUE) FDA UDI

Identifiers

Catalog Number
TS FM-B24141 FDA UDI
Primary DI / UDI-DI
00723860241412 FDA UDI
FDA Product Code
FXX FDA UDI
GMDN Term
Surgical/medical face mask, non-antimicrobial, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical/medical face mask, non-antimicrobial, single-use

The Sea by Mexpo International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/medical face mask, non-antimicrobial, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mexpo International, Inc.

Sources (1)

  • FDA UDI a4bdfa8a-2b82-4c49-ba01-a9ca1185e8f6 34 fields · synced Jun 8, 2026