← Back to catalogue

Vguard

FDA UDI

Class I (US FDA UDI)

by Vanguard International Solutions, LLC

Identity

Trade Name
VGUARD FDA UDI
Generic Name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
Nitrile Exam PF Blue 10/90 2X FDA UDI
Model / Reference
A11A15 FDA UDI
Description
Nitrile Exam PF Blue 10/90 2X FDA UDI

Identifiers

Primary DI / UDI-DI
00810052977522 FDA UDI
510(k) Number
K092874 FDA UDI
K131440 FDA UDI
K210684 FDA UDI
FDA Product Code
LZA 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

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: Nitrile examination/treatment glove, non-powdered, non-antimicrobial

Vguard by Vanguard International Solutions, 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.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 4243d0d8-a1ea-44b1-8708-157c373238a4 34 fields · synced Jun 8, 2026