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Med-Defend

FDA UDI

Class I (US FDA UDI)

by Seattle Glove, Inc.

Identity

Trade Name
MED-DEFEND FDA UDI
Generic Name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
HIGH RISK NITRILE POWDER FREE MEDICAL EXAM GLOVES, 50/BOX, LONG CUFF, M, TESTED FOR USE WITH CHEMOTHERAPY DRUGS, FENTANYL RESISTANT FDA UDI
Model / Reference
V908MPF-M-BX FDA UDI
Description
HIGH RISK NITRILE POWDER FREE MEDICAL EXAM GLOVES, 50/BOX, LONG CUFF, M, TESTED FOR USE WITH CHEMOTHERAPY DRUGS, FENTANYL RESISTANT FDA UDI

Identifiers

Primary DI / UDI-DI
00850046285493 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

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

Yes

FDA UDI

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

Med-Defend by Seattle Glove, 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
Seattle Glove, Inc.

Sources (1)

  • FDA UDI 75d62ffa-4666-44c7-a2d1-6368815ab41d 33 fields · synced May 30, 2026