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

52313A — Class I MDR by Brainlab SE

MD Atlas
Brainlab SE

EUDAMED last updated this device on Jun 12, 2025

52313A

4056481SteriTrayRF

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Brainlab SE
UDI-DI code: 04056481095390
Reference / catalog number: 52313A

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

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW011
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.

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: 04056481095390
Basic UDI-DI: 4056481SteriTrayRF
Reference / catalog number: 52313A
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: No clinical sizes registered for this device.

EMDN nomenclature code(s)

S010499STERILISATION CONTAINERS - OTHER

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

Certificates

Certificate health across this manufacturer's portfolio.

G70 037489 0071Issued
Technical documentationNotified body: 0123Expiry: Mar 15, 2028
G70 037489 0072Issued
Technical documentationNotified body: 0123Expiry: Mar 13, 2028

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 ARRAY4056481PatRefXPress35

On the market