← Back to catalogue

Blossom Latex Examination Gloves Textured Powder Free

EUDAMEDFDA UDI

Class I (EU MDR)

Ref BM 6225-LTX PFModel LATEX EXAMINATION GLOVES POWDER FREE

by Mexpo International, Inc.

Identity

Trade Name
BLOSSOM LATEX EXAMINATION GLOVES TEXTURED POWDER FREE EUDAMED
BLOSSOM FDA UDI
Generic Name
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
LATEX EXAMINATION GLOVES POWDER FREE EUDAMED
LATEX EXAMINATION GLOVES TEXTURED POWDER FREE (X-SMALL) FDA UDI
Model / Reference
LATEX EXAMINATION GLOVES POWDER FREE EUDAMED
BM 6225-LTX PF EUDAMEDFDA UDI
Description
LATEX EXAMINATION GLOVES TEXTURED POWDER FREE (X-SMALL) FDA UDI

Identifiers

Catalog Number
BM 6225-LTX PF FDA UDI
Primary DI / UDI-DI
00723860062253 EUDAMEDFDA UDI
Basic UDI-DI
0723860471728V EUDAMED
FDA Product Code
LYY FDA UDI
EMDN Code
T010201 LATEX EXAMINATION / TREATMENT GLOVES EUDAMED
GMDN Term
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.6250 FDA UDI
Market of Registration
Spain EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

Yes

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Blossom Latex Examination Gloves Textured Powder Free by Mexpo International, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000032548
Authorised Representative
Blossom Europe, S.L. ES-AR-000019689

Sources (2)

  • EUDAMED 5fa3a503-949c-4618-8de7-9199dff665f5 61 fields · synced Jun 18, 2026
  • FDA UDI 0993a713-a5f4-4287-b218-1513f42be935 34 fields · synced May 30, 2026