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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

04-GCR007 — Class I MDR by "Gamma" Medizinisch-wiss…

MD Atlas
"Gamma" Medizinisch-wissenschaftliche Fortbildungs GmbH

EUDAMED last updated this device on Feb 7, 2023

04-GCR007

912012191FBKINXF

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: "Gamma" Medizinisch-wissenschaftliche Fortbildungs GmbH
UDI-DI code: 09120121910123
Reference / catalog number: 04-GCR007

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Manufacturer information

Organization name: "Gamma" Medizinisch-wissenschaftliche Fortbildungs GmbH
SRN: AT-MF-000004222
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW018
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Austria; available across 1 country total.

Placed on the market in Austria; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 09120121910123
Basic UDI-DI: 912012191FBKINXF
Reference / catalog number: 04-GCR007
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Der Condylograph Gesichtsbogen ist notwendiges Zubehör zum CADIAX System. An dem Gesichtsbogen werden die Flaggen und Styli des CADIAX Systems befestigt. Des Weiteren wird mit dem Gesichtsbogen die Kieferrelationsbestimmung, d.h. die Bestimmung der Lage der Kiefer zu einer Referenzebene, durchgeführt. Diese Kieferrelationsbestimmung ist für eine lagegerechte Montage der Kiefermodelle im Artikulator erforderlich.
Additional information URL: https://www.gammadental.com/de/downloads.html
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q010401ORTHODONTIC FACE BOWS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.