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Protect

EUDAMED

Class I (EU MDR)

Ref PB (G2)

by Axg Industries Sdn Bhd

Identity

Trade Name
PROTECT EUDAMED
Device Name
Powder Free Latex Examination Glove, Black Color Non-Sterile EUDAMED
Model / Reference
PB (G2) EUDAMED

Identifiers

Primary DI / UDI-DI
95557100013860 EUDAMED
Basic UDI-DI
95557100013860TK EUDAMED
Direct Marketing DI
95557100013860 EUDAMED
EMDN Code
T010201 LATEX EXAMINATION / TREATMENT GLOVES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

EUDAMED

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

Protect by Axg Industries Sdn Bhd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
MY-MF-000018723
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 2a111179-d234-4998-ba06-0635fd719998 61 fields · synced Jun 18, 2026