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

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Organization name
UDI-DI code
Reference / catalog number

PADERECOFRESH2E — Class I MDR by Pader Medi.Tech GmbH &…

MD Atlas
Pader Medi.Tech GmbH & Co. KG

EUDAMED last updated this device on Mar 6, 2026

PADERECOFRESH2E

42513093PADERECOFRESH2EEZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Pader Medi.Tech GmbH & Co. KG
UDI-DI code: 04251309332866
Reference / catalog number: PADERECOFRESH2E

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Manufacturer information

Organization name: Pader Medi.Tech GmbH & Co. KG
SRN: DE-MF-000018541
Manufacturer status: Active

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: 04251309332866
Basic UDI-DI: 42513093PADERECOFRESH2EEZ
Reference / catalog number: PADERECOFRESH2E
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: Die Behandlungsliege dient dazu, unter Anleitung eines Therapeuten bestimmte Körperhaltungen zu ermöglichen.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08060199ELECTRIC MEDICAL BEDS - 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

Related devices

This device is not currently linked to any other device.

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.