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DORO® Horseshoe Pad, Adult, left

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 3009-11

by Black Forest Medical GmbH

Identity

Trade Name
DORO® Horseshoe Pad, Adult, left EUDAMED
DORO® Horseshoe Pad FDA UDI
Generic Name
Neurosurgical headrest FDA UDI
Device Name
Headrestsystem Imaging EUDAMED
DORO® Horseshoe Pad, Adult, left FDA UDI
Model / Reference
3009-11 EUDAMEDFDA UDI
Description
DORO® Horseshoe Pad, Adult, left FDA UDI

Identifiers

Primary DI / UDI-DI
04250435501283 EUDAMEDFDA UDI
Basic UDI-DI
42504355PA01EH EUDAMED
Direct Marketing DI
04250435501283 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Orthopaedic trocar blade, reusable

DORO® Horseshoe Pad, Adult, left 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

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Manufacturer

EUDAMED SRN
DE-MF-000005752

Sources (2)

  • EUDAMED 78f6012c-7eaf-4b2e-8bb1-1e91464a26db 61 fields · synced Jul 10, 2026
  • FDA UDI 88b323e6-9bb0-4c71-aaca-76697e1fa339 34 fields · synced May 25, 2026