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Typ F 7

EUDAMED

Class I (EU MDR)

Ref 8700

by Ultradent Dental-Medizinische-Geräte GmbH & Co KG

Identity

Trade Name
Typ F 7 EUDAMED
Device Name
Fußanlasser EUDAMED
Model / Reference
8700 EUDAMED

Identifiers

Primary DI / UDI-DI
04260746660289 EUDAMED
Basic UDI-DI
426074666UD733036X EUDAMED
Direct Marketing DI
04260746660289 EUDAMED
EMDN Code
Z12110101 DENTAL TREATMENT UNITS 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

Typ F 7 by Ultradent Dental-Medizinische-Geräte GmbH & Co KG — 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
DE-MF-000020027

Sources (1)

  • EUDAMED 0c2730ed-69f3-4864-b2e0-54b6ec711a94 61 fields · synced Jun 18, 2026