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

2152175 — Class I MDR by Besco Medical Medizin-…

MD Atlas
Besco Medical Medizin- und Rehaprodukte GmbH

EUDAMED last updated this device on Dec 13, 2024

2152175

4260685532000XG

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Besco Medical Medizin- und Rehaprodukte GmbH
UDI-DI code: 42606855306128
Reference / catalog number: 2152175

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: Besco Medical Medizin- und Rehaprodukte GmbH
SRN: DE-MF-000008152
Manufacturer status: Active

Related devices

42606855348184260685534000XWOn the market 42606855348254260685534000XWOn the market 42606855348324260685534000XWOn the market 70605704260685531000X9On the market 70609704260685531000X9On 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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

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: 42606855306128
Basic UDI-DI: 4260685532000XG
Reference / catalog number: 2152175
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: Der Rollstuhl Primus ML 2.0 ist für den Innen- und Außenbereich konzipiert. Er ist ausschließlich zur Selbst- und Fremdbeförderung von einer Person gedacht. Der Rollstuhl ist auf eine maximale Belastung von 130 kg ausgelegt.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y122106REAR SELF-PROPELLED WHEELCHAIRS

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