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Asp Medical

FDA UDI

Class I (US FDA UDI)

by Asp Global, LLC

Identity

Trade Name
ASP MEDICAL FDA UDI
Generic Name
Non-adhesive device retention bandage FDA UDI
Device Name
BULKY GAUZE BANDAGE, 6PLY, 4.5"X4.1YD, NON STERILE FDA UDI
Model / Reference
NPT146 FDA UDI
Description
BULKY GAUZE BANDAGE, 6PLY, 4.5"X4.1YD, NON STERILE FDA UDI

Identifiers

Primary DI / UDI-DI
00840216103795 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Non-adhesive device retention bandage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 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

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-adhesive device retention bandage

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

Similar devices

Also classified as Non-adhesive device retention bandage.

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 e5b0c52f-a335-48b8-a147-767d44429839 33 fields · synced May 30, 2026