← Back to catalogue
Blossom Latex Examination Gloves Powder Free With Aloe Vera
EUDAMEDFDA UDIClass I (EU MDR)
Ref BM 11227-PF-AVModel LATEX EXAMINATION GLOVES POWDER FREE
Identity
- Trade Name
- BLOSSOM LATEX EXAMINATION GLOVES POWDER FREE WITH ALOE VERA EUDAMEDBLOSSOM FDA UDI
- Generic Name
- Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
- Device Name
- LATEX EXAMINATION GLOVES POWDER FREE EUDAMEDLATEX EXAMINATION GLOVES POWDER FREE WITH ALOE VERA MEDIUM) FDA UDI
- Model / Reference
- LATEX EXAMINATION GLOVES POWDER FREE EUDAMEDBM 11227-PF-AV EUDAMEDFDA UDI
- Description
- LATEX EXAMINATION GLOVES POWDER FREE WITH ALOE VERA MEDIUM) FDA UDI
Identifiers
- Catalog Number
- BM 11227-PF-AV FDA UDI
- Primary DI / UDI-DI
- 00723860112279 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 Powder Free With Aloe Vera 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0723860471728V | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Mexpo International, Inc.
- EUDAMED SRN
- US-MF-000032548
- Authorised Representative
- Blossom Europe, S.L. ES-AR-000019689
Sources (2)
- EUDAMED 5a2ee6f9-a3ae-47e1-afc6-c7ed2b55ae16 61 fields · synced Jul 9, 2026
- FDA UDI 1ae834df-f336-44e4-97fd-3589b3c6c780 34 fields · synced May 30, 2026