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Bosma Enterprises

FDA UDI

Class I (US FDA UDI)

by Bosma Enterprises

Identity

Trade Name
Bosma Enterprises FDA UDI
Generic Name
Vinyl examination/treatment glove, non-powdered FDA UDI
Device Name
Vinyl Powder Free Exam Gloves Medium 100/Box FDA UDI
Model / Reference
72-90602 FDA UDI
Description
Vinyl Powder Free Exam Gloves Medium 100/Box FDA UDI

Identifiers

Catalog Number
72-90602 FDA UDI
Primary DI / UDI-DI
20818634020042 FDA UDI
510(k) Number
K070076 FDA UDI
FDA Product Code
LYZ FDA UDI
GMDN Term
Vinyl examination/treatment glove, non-powdered 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vinyl examination/treatment glove, non-powdered

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

Similar devices

Also classified as Vinyl examination/treatment glove, non-powdered.

Cleared under the same submission

K070076 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bosma Enterprises

Sources (1)

  • FDA UDI 6165d6c7-5d45-4bff-b4d2-675954b89bf9 38 fields · synced Jun 1, 2026