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DORO® Adaptor for Flat Brain Spatula

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 1201.046

by Black Forest Medical GmbH

Identity

Trade Name
DORO® Adaptor for Flat Brain Spatula EUDAMED
DORO® Adaptor FDA UDI
Generic Name
Surgical retraction system, reusable FDA UDI
Device Name
Retractor System EUDAMED
DORO® Adaptor for Flat Brain Spatula FDA UDI
Model / Reference
1201.046 EUDAMEDFDA UDI
Description
DORO® Adaptor for Flat Brain Spatula FDA UDI

Identifiers

Primary DI / UDI-DI
04250435519189 EUDAMEDFDA UDI
Basic UDI-DI
42504355PA04EP EUDAMED
Direct Marketing DI
04250435519189 EUDAMED
510(k) Number
K001808 FDA UDI
FDA Product Code
HBL FDA UDI
EMDN Code
Z12109080 VARIOUS NEUROLOGY AND NEUROSURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Surgical retraction system, reusable 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

Category: Orthopaedic trocar blade, reusable

DORO® Adaptor for Flat Brain Spatula 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 e94430a3-0af7-41eb-9f3b-93b9f67a3209 61 fields · synced Jun 18, 2026
  • FDA UDI 3e2708ca-97ad-4cd9-b22b-66aff85ebfd3 34 fields · synced May 26, 2026