← Back to catalogue

Ultrasound Navigation Adapter Generic

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 41860-42

by Brainlab SE

Identity

Trade Name
ULTRASOUND NAVIGATION ADAPTER GENERIC EUDAMED
GENERIC ULTRASOUND ADAPTER BASE FDA UDI
Generic Name
Robotic surgical navigation system FDA UDI
Device Name
ULTRASOUND NAVIGATION ADAPTER GENERIC EUDAMED
Model / Reference
41860-42 EUDAMEDFDA UDI

Identifiers

Catalog Number
41860-42 FDA UDI
Primary DI / UDI-DI
04056481141387 EUDAMEDFDA UDI
Basic UDI-DI
4056481USNavAdapter9Y EUDAMED
Direct Marketing DI
04056481141387 EUDAMED
510(k) Number
K092467 FDA UDI
K192703 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Neurological stereotactic surgery system

Ultrasound Navigation Adapter Generic by Brainlab SE — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Brainlab SE
EUDAMED SRN
DE-MF-000006183

Sources (2)

  • EUDAMED f5adb7b5-3305-466c-a66b-6a59b96379f0 61 fields · synced Aug 3, 2026
  • FDA UDI 167735a6-ee05-40be-92b9-69f13058c420 35 fields · synced May 30, 2026