← Back to catalogue

Protexis

FDA UDI

Class I (US FDA UDI)

by Bosma Enterprises

Identity

Trade Name
Protexis FDA UDI
Generic Name
Polyisoprene surgical glove, non-powdered, non-antimicrobial FDA UDI
Device Name
Protexis PI Surgical 7.5 - 50 Pair/Box FDA UDI
Model / Reference
71-2D72PT75 FDA UDI
Description
Protexis PI Surgical 7.5 - 50 Pair/Box FDA UDI

Identifiers

Catalog Number
71-2D72PT75 FDA UDI
Primary DI / UDI-DI
10818634021974 FDA UDI
FDA Product Code
KGO FDA UDI
GMDN Term
Polyisoprene surgical glove, non-powdered, non-antimicrobial 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Polyisoprene surgical glove, non-powdered, non-antimicrobial

Protexis by Bosma Enterprises — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyisoprene surgical glove, non-powdered, non-antimicrobial.

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

Manufacturer
Bosma Enterprises

Sources (1)

  • FDA UDI aead830a-5a80-43e4-9436-a2d5bc12e9a8 37 fields · synced Jun 1, 2026