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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

70-520-02 — Class IIa MDR by M.I.S.S. Medizintechnik…

MD Atlas
M.I.S.S. Medizintechnik GmbH

EUDAMED last updated this device on Jul 25, 2025

70-520-02

426072983PRPLH

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: M.I.S.S. Medizintechnik GmbH
UDI-DI code: 04260729832030
Reference / catalog number: 70-520-02

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Manufacturer information

Organization name: M.I.S.S. Medizintechnik GmbH
SRN: DE-MF-000020722
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Apr 2, 2001	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260729832030
Basic UDI-DI: 426072983PRPLH
Reference / catalog number: 70-520-02
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Invidia Uro-Pump (BU-U)
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12019007IRRIGATORS

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

71-435-00426072983PRPLHOn the market 70-520-00426072983PRPLHOn the market UNT-16-006426072983PRPLHOn the market 70520-04426072983PRPLHOn the market 1143-2426072983PRPLHOn 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.