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ResQ-Grip

FDA UDI

Class I (US FDA UDI)

by Summit Glove Inc.

Identity

Trade Name
ResQ-Grip FDA UDI
Generic Name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
5mil, 9.5" in Length, Ambidextrous, Examination Grade Glove, Powder Free, Raised Diamond Pattern, Beaded Cuff, Blue, Size X-Large FDA UDI
Model / Reference
79750PF-RBGR FDA UDI
Description
5mil, 9.5" in Length, Ambidextrous, Examination Grade Glove, Powder Free, Raised Diamond Pattern, Beaded Cuff, Blue, Size X-Large FDA UDI

Identifiers

Primary DI / UDI-DI
00850019992021 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
Not 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

ResQ-Grip by Summit Glove Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Summit Glove Inc.

Sources (1)

  • FDA UDI 965529cb-50a6-4fb3-85b9-2f57d17b6da5 35 fields · synced Jun 1, 2026