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Target Up&Up

FDA UDI

Class I (US FDA UDI)

by Armbrust, Inc.

Identity

Trade Name
Target Up&Up FDA UDI
Generic Name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
USA Made Nitrile Gloves - Blue - Medium - Box of 50 FDA UDI
Model / Reference
GLOVE-ARMBRUST-3.9MIL-BLUE-BOX-1X50-M FDA UDI
Description
USA Made Nitrile Gloves - Blue - Medium - Box of 50 FDA UDI

Identifiers

Primary DI / UDI-DI
00850056441209 FDA UDI
510(k) Number
K222898 FDA UDI
FDA Product Code
LZA FDA UDI
LZC 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

Yes

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

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

Target Up&Up by Armbrust, Inc. — 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
Armbrust, Inc.

Sources (1)

  • FDA UDI 16f88fe9-a767-4db7-9c72-7221073dd02d 36 fields · synced May 30, 2026