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DORO® LUCENT iMRI Interface Adaptor IMRIS

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 4003.611

by Black Forest Medical GmbH

Identity

Trade Name
DORO® LUCENT iMRI Interface Adaptor IMRIS EUDAMEDFDA UDI
Generic Name
Medical table clamp FDA UDI
Device Name
Headrestsystem for MR imaging EUDAMED
DORO® LUCENT iMRI Interface Adaptor IMRIS FDA UDI
Model / Reference
4003.611 EUDAMEDFDA UDI
Description
DORO® LUCENT iMRI Interface Adaptor IMRIS FDA UDI

Identifiers

Primary DI / UDI-DI
04250435539521 EUDAMEDFDA UDI
Basic UDI-DI
42504355PA05ER EUDAMED
Direct Marketing DI
04250435539521 EUDAMED
FDA Product Code
JEA FDA UDI
EMDN Code
Z12109080 VARIOUS NEUROLOGY AND NEUROSURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Medical table clamp FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4960 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Orthopaedic trocar blade, reusable

DORO® LUCENT iMRI Interface Adaptor IMRIS by Black Forest Medical GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic trocar blade, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000005752

Sources (2)

  • EUDAMED 9e64c323-1eb9-4122-809d-f418f9b63ecd 61 fields · synced Oct 6, 2026
  • FDA UDI 1b0e5710-6577-4bc8-8fe9-e579aa5d91c6 33 fields · synced May 30, 2026