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Alpha-Ease 7 Ml Desensitizer

EUDAMED

Class IIa (EU MDR)

Ref 408-0101-002

by Dental Technologies, Inc.

Identity

Trade Name
ALPHA-EASE 7 ML DESENSITIZER EUDAMED
Device Name
Desensitizer EUDAMED
Model / Reference
408-0101-002 EUDAMED

Identifiers

Primary DI / UDI-DI
+D73540801010020 EUDAMED
Basic UDI-DI
++D735DesensitizerNP EUDAMED
EMDN Code
Q019008 DENTINAL DESENSITISERS EUDAMED

Classification

Device Class
Class IIa 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

Alpha-Ease 7 Ml Desensitizer by Dental Technologies, Inc. — Class IIa — 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
US-MF-000027130
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 6a992b7d-45e7-4471-aeb1-9029cec25b6c 61 fields · synced Jul 12, 2026