Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

41839-52 — Class I MDR by Brainlab SE

MD Atlas
Brainlab SE

EUDAMED last updated this device on May 21, 2024

41839-52

4056481DrillGuideDU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Brainlab SE
UDI-DI code: 04056481141516
Reference / catalog number: 41839-52

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: Brainlab SE
SRN: DE-MF-000006183
Manufacturer status: Active

Related devices

19153-044056481RadiolBaAdaInterPJOn the market ADAPTER FOR SURGICAL MOTOR SYSTEM4056481AdapterMotor6KOn the market 55761-02A4056481PatRefAdapterJSOn the market 55761-01B4056481PatRefAdapterJSOn the market ADAPTER X-PRESS FOR PATIENT REFERENCE ARRAY4056481PatRefXPress35On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04056481141516
Basic UDI-DI: 4056481DrillGuideDU
Reference / catalog number: 41839-52
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 99.5–151.5 MU50

EMDN nomenclature code(s)

Z12011480SURGICAL NAVIGATION INSTRUMENTS - HARDWARE ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification