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Radiolucent Drapelink Interface For Calibration Phantom Intraoperative Ct

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 19142-06

by Brainlab SE

Identity

Trade Name
RADIOLUCENT DRAPELINK INTERFACE FOR CALIBRATION PHANTOM INTRAOPERATIVE CT EUDAMED
Drapelink Interface Ict Calib Phantom FDA UDI
Generic Name
Robotic surgical navigation system FDA UDI
Device Name
Calibration Phantom Interoperative CT EUDAMED
Model / Reference
19142-06 EUDAMEDFDA UDI

Identifiers

Catalog Number
19142-06 FDA UDI
Primary DI / UDI-DI
04056481004637 EUDAMEDFDA UDI
Basic UDI-DI
4056481CaliPhantomICTHC EUDAMED
Direct Marketing DI
04056481004637 EUDAMED
510(k) Number
K092467 FDA UDI
K192703 FDA UDI
K234047 FDA UDI
K252562 FDA UDI
FDA Product Code
HAW FDA UDI
EMDN Code
Z12011480 SURGICAL NAVIGATION INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Robotic surgical navigation system FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
882.4560 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
MRI Safety
MR Conditional FDA UDI

Category: Neurological stereotactic surgery system

Radiolucent Drapelink Interface For Calibration Phantom Intraoperative Ct by Brainlab SE — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Neurological stereotactic surgery system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Brainlab SE
EUDAMED SRN
DE-MF-000006183

Sources (2)

  • EUDAMED b81a771f-2184-46f6-882a-58b9af5e8b50 61 fields · synced Jun 19, 2026
  • FDA UDI 409ab33d-a7b9-4491-abe2-2853b8874c57 35 fields · synced May 30, 2026