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Calibration Sources

EUDAMED

Class I (EU MDR)

Ref BM06E-37-100

by Radnostix, Inc.

Identity

Device Name
Calibration Sources EUDAMED
Model / Reference
BM06E-37-100 EUDAMED

Identifiers

Primary DI / UDI-DI
00810212891330 EUDAMED
Basic UDI-DI
0081021289CALIBRATIONYU EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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: Device sterilization/disinfection container, reusable

Calibration Sources by Radnostix — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Radnostix, Inc.
EUDAMED SRN
US-MF-000009369
Authorised Representative
CERT3GLOBAL, UNIPESSOAL, LDA. PT-AR-000037982

Sources (1)

  • EUDAMED 4f64e114-7267-49c4-bcde-0fcae3329cf5 61 fields · synced Jul 31, 2026