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

CLPESDHLRMG — Class I MDR by Lehnen GmbH

MD Atlas
Lehnen GmbH

EUDAMED last updated this device on Sep 8, 2022

CLPESDHLRMG

4250365200001QJ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Lehnen GmbH
UDI-DI code: 04250365216882
Reference / catalog number: CLPESDHLRMG

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: Lehnen GmbH
SRN: DE-MF-000025229
Manufacturer status: Active

Related devices

L10521224250365200001QJOn the market L10521124250365200001QJOn the market L10521214250365200001QJOn the market L10521114250365200001QJOn the market L10521244250365200001QJOn 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.

CW018
Montageanleitung beachten!

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: 04250365216882
Basic UDI-DI: 4250365200001QJ
Reference / catalog number: CLPESDHLRMG
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: Duschhandläufe werden rund um Badewanne, Dusche und Waschtisch eingesetzt. Sie dienen dabei als Ein- und Ausstiegshilfe und sorgen für einen sicheren Halt.
Additional information URL: https://www.vigour.de/service/katalogregal
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y181806HANDLES

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