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MedPride

FDA UDI

Class I (US FDA UDI)

by Shield-Line, Llc

Identity

Trade Name
MedPride FDA UDI
Generic Name
Nitrile surgical glove, non-powdered FDA UDI
Device Name
Intended to be used in surgery for patients and user FDA UDI
Model / Reference
SIZE 8.0 FDA UDI
Description
Intended to be used in surgery for patients and user FDA UDI

Identifiers

Catalog Number
MPR-51616 FDA UDI
Primary DI / UDI-DI
10352410516167 FDA UDI
510(k) Number
K122557 FDA UDI
FDA Product Code
KGO FDA UDI
GMDN Term
Nitrile surgical glove, non-powdered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4460 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nitrile surgical glove, non-powdered

MedPride by Shield-Line, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nitrile surgical glove, non-powdered.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shield-Line, Llc

Sources (1)

  • FDA UDI d49b40d3-c6e3-45e8-bd22-c29534fad10a 35 fields · synced Jun 7, 2026