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Tinearity G1

EUDAMED

Class IIa (EU MDR)

Ref 6006Model G1

by Circius Pharma AB

Identity

Trade Name
Tinearity G1 EUDAMED
Device Name
Tinearity EUDAMED
Model / Reference
G1 EUDAMED
6006 EUDAMED

Identifiers

Primary DI / UDI-DI
07350133961109 EUDAMED
Basic UDI-DI
735013396Tinearity1Z5 EUDAMED
Direct Marketing DI
07350133961109 EUDAMED
EMDN Code
Z129013 GENERAL AUDITORY AND/OR VISUAL STIMULATORS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Sweden 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: Auditory stimulator

Tinearity G1 by Circius Pharma AB — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Auditory stimulator.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Circius Pharma AB
EUDAMED SRN
SE-MF-000013023

Sources (1)

  • EUDAMED 916e6d4d-de36-4b84-96e8-d5cfc62b462d 61 fields · synced Jun 18, 2026