Asp Medical

FDA UDI

Class I (US FDA UDI)

by Asp Global, LLC

Identity

Trade Name: ASP MEDICAL FDA UDI
Generic Name: Pressure bandage, non-latex, single-use FDA UDI
Device Name: ESMARK NONSTERILE LATEX FREE 6" X 12' BLUE, 1/EA,20/CS FDA UDI
Model / Reference: EST162 FDA UDI
Description: ESMARK NONSTERILE LATEX FREE 6" X 12' BLUE, 1/EA,20/CS FDA UDI

Identifiers

Primary DI / UDI-DI: 00840216102422 FDA UDI
FDA Product Code: FQM FDA UDI
GMDN Term: Pressure bandage, non-latex, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5075 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Pressure bandage, non-latex, single-use

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Asp Global, LLC

Sources (1)

FDA UDI 8b98a960-6231-4b6f-bfae-ea1355634014 33 fields · synced May 31, 2026