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Blossom

FDA UDI

Class I (US FDA UDI)

by Mexpo International, Inc.

Identity

Trade Name
BLOSSOM FDA UDI
Generic Name
Vinyl examination/treatment glove, non-powdered FDA UDI
Device Name
VINYL EXAMINATION GLOVES POWDER FREE WHITE (X-SMALL) FDA UDI
Model / Reference
BM 5225-WOP-PF FDA UDI
Description
VINYL EXAMINATION GLOVES POWDER FREE WHITE (X-SMALL) FDA UDI

Identifiers

Catalog Number
BM 5225-WOP-PF FDA UDI
Primary DI / UDI-DI
00723860052254 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Vinyl examination/treatment glove, non-powdered

Blossom by Mexpo International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 37989114-e8b8-4cc1-a86d-8d19b9e7445f 34 fields · synced Jun 8, 2026