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DORO® Horsehoe Headrest, Adult, radiolucent with Extension Bar

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 3036-50

by Black Forest Medical GmbH

Identity

Trade Name
DORO® Horsehoe Headrest, Adult, radiolucent with Extension Bar EUDAMED
DORO® Horseshoe radiolucent FDA UDI
Generic Name
Neurosurgical headrest FDA UDI
Device Name
Headrestsystem Imaging EUDAMED
DORO® Horsehoe Headrest, Adult, radiolucent with Extension Bar FDA UDI
Model / Reference
3036-50 EUDAMEDFDA UDI
Description
DORO® Horsehoe Headrest, Adult, radiolucent with Extension Bar FDA UDI

Identifiers

Primary DI / UDI-DI
04250435502358 EUDAMEDFDA UDI
Basic UDI-DI
42504355PA01EH EUDAMED
Direct Marketing DI
04250435502358 EUDAMED
510(k) Number
K032331 FDA UDI
K063494 FDA UDI
FDA Product Code
HBL FDA UDI
EMDN Code
Z12109080 VARIOUS NEUROLOGY AND NEUROSURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Neurosurgical headrest FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
882.4460 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

DORO® Horsehoe Headrest, Adult, radiolucent with Extension Bar by Black Forest Medical GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

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 6d0643d8-8e52-4399-b6f3-01eccf731081 61 fields · synced Oct 6, 2026
  • FDA UDI 768935a1-35c0-4a79-93e6-450b56158153 34 fields · synced May 30, 2026