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DORO® Torx Screwdriver T45, nonmagnetic (1 pcs)

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 3033-68

by Black Forest Medical GmbH

Identity

Trade Name
DORO® Torx Screwdriver T45, nonmagnetic (1 pcs) EUDAMED
DORO® Torx Screwdriver FDA UDI
Generic Name
Skull clamp FDA UDI
Device Name
Headrestsystem for MR imaging EUDAMED
DORO® Torx Screwdriver T45, nonmagnetic FDA UDI
Model / Reference
3033-68 EUDAMEDFDA UDI
Description
DORO® Torx Screwdriver T45, nonmagnetic FDA UDI

Identifiers

Primary DI / UDI-DI
04250435528273 EUDAMEDFDA UDI
Basic UDI-DI
42504355PA05ER 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
Skull clamp 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 Conditional FDA UDI

Category: Orthopaedic trocar blade, reusable

DORO® Torx Screwdriver T45, nonmagnetic (1 pcs) by Black Forest Medical GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

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 30e83bc5-b8b4-40e5-badd-298f8d56854c 61 fields · synced Oct 6, 2026
  • FDA UDI d257ae3f-37c3-44ae-a1c7-7fcd45796cd1 34 fields · synced May 30, 2026