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Asp Global

FDA UDI

Class I (US FDA UDI)

by Asp Global, LLC

Identity

Trade Name
ASP GLOBAL FDA UDI
Generic Name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
GLOVES, PROTECTIVEFIT NITRILE BIODEGRADABLE, CHEMO-RATED, SMALL, BLUE, 200EA/BX, 10BX/CS (2000EA/CS) FDA UDI
Model / Reference
PFG200S-BIO FDA UDI
Description
GLOVES, PROTECTIVEFIT NITRILE BIODEGRADABLE, CHEMO-RATED, SMALL, BLUE, 200EA/BX, 10BX/CS (2000EA/CS) FDA UDI

Identifiers

Primary DI / UDI-DI
00840216123311 FDA UDI
FDA Product Code
LZA FDA UDI
LZC FDA UDI
QDO FDA UDI
OPJ FDA UDI
GMDN Term
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6250 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: Nitrile examination/treatment glove, non-powdered, non-antimicrobial

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

Similar devices

Also classified as Nitrile examination/treatment glove, non-powdered, non-antimicrobial.

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 0723fd6f-2bcb-443c-a110-477490728c1b 33 fields · synced May 31, 2026