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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

3031.5.00 — Class I MDR by Hydas GmbH & Co. KG

MD Atlas
Hydas GmbH & Co. KG

EUDAMED last updated this device on Apr 28, 2026

3031.5.00

4004128BeckenbodentrainB7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Hydas GmbH & Co. KG
UDI-DI code: 04004128017816
Reference / catalog number: 3031.5.00

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Manufacturer information

Organization name: Hydas GmbH & Co. KG
SRN: DE-MF-000016598
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW999
Nach frischen Operationen insbesondere im Beckenbodenbereich, sollte das Training nur nach Rücksprache mit dem behandelnden Arzt begonnen werden. Wie lange nach einer Operation die entsprechenden Muskeln noch geschont werden sollen entscheidet der Arzt.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	Apr 28, 2026	Jul 23, 2026
Austria	Apr 28, 2026	Jul 23, 2026

Device identification

Trade name: not provided
UDI-DI code: 04004128017816
Basic UDI-DI: 4004128BeckenbodentrainB7
Reference / catalog number: 3031.5.00
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)

T0499INCONTINENCE DEVICES - 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

9681.5.004004128BeckenbodentrainB7On the market 9681.1.004004128BeckenbodentrainB7On the market 1501.1.014004128GeradehalterQYOn the market 3001.1.004004128InhalatorZ2On the market 9690.1.004004128InhalatorZ2On 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.