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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

KRGES — Class I MDR by HP Velotechnik GmbH &…

MD Atlas
HP Velotechnik GmbH & Co. KG

EUDAMED last updated this device on May 20, 2026

KRGES

42512209TherapieraederW8

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: HP Velotechnik GmbH & Co. KG
UDI-DI code: 04251220909833
Reference / catalog number: KRGES

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Manufacturer information

Organization name: HP Velotechnik GmbH & Co. KG
SRN: DE-MF-000030326
Manufacturer status: Active

Critical warnings

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

CW018
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04251220909833
Basic UDI-DI: 42512209TherapieraederW8
Reference / catalog number: KRGES
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)

Y121809MANUALLY PROPELLED TRICYCLES

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

KREGES42512209TherapieraederW8On the market KRGELH42512209TherapieraederW8On the market KREGELH42512209TherapieraederW8On the market KRSFSH42512209TherapieraederW8On the market KRESFSH42512209TherapieraederW8On 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.