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Asp Medical

FDA UDI

Class II (US FDA UDI)

by Asp Global, LLC

Identity

Trade Name
ASP MEDICAL FDA UDI
Generic Name
Surgical/medical face mask, single-use FDA UDI
Device Name
MASK, FACE, BLUE, EARLOOPS, TESTED TO ASTM F1862 (FLUID PROTECTION BARRIER) LEVEL 3 FDA UDI
Model / Reference
FMT650 FDA UDI
Description
MASK, FACE, BLUE, EARLOOPS, TESTED TO ASTM F1862 (FLUID PROTECTION BARRIER) LEVEL 3 FDA UDI

Identifiers

Primary DI / UDI-DI
00840216108646 FDA UDI
FDA Product Code
FXX FDA UDI
GMDN Term
Surgical/medical face mask, 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

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: Surgical/medical face mask, single-use

Asp Medical by Asp Global, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Asp Global, LLC

Sources (1)

  • FDA UDI 957615a4-eaa8-45a0-b088-b58e3c9e791f 33 fields · synced May 31, 2026