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BA Alginate Mixer

EUDAMED

Class I (EU MDR)

Ref BASE900

by B.A. International Ltd

Identity

Trade Name
BA Alginate Mixer EUDAMED
Device Name
BA Alginate Mixer EUDAMED
Model / Reference
BASE900 EUDAMED

Identifiers

Primary DI / UDI-DI
05060493661527 EUDAMED
Basic UDI-DI
506049366BAAI6U EUDAMED
EMDN Code
Q010207 DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

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

Category: Dental implant suprastructure, temporary, preformed, single-use

BA Alginate Mixer by B.A. International Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
GB-MF-000033489
Authorised Representative
CB Healthcare Consulting GmbH DE-AR-000005903

Sources (1)

  • EUDAMED 695625ff-3042-473d-ba65-ea3746ed46b3 61 fields · synced Jun 20, 2026