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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

HC, HP, HU — Class I MDR by Hageneder Medizintechnik…

MD Atlas
Hageneder Medizintechnik GmbH

EUDAMED last updated this device on Mar 4, 2026

HC, HP, HU

912012039disposalsystemYD

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Hageneder Medizintechnik GmbH
UDI-DI code: 09120120390025
Reference / catalog number: HC, HP, HU

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Manufacturer information

Organization name: Hageneder Medizintechnik GmbH
SRN: AT-MF-000003630
Manufacturer status: Active

Market distribution

Primary placement in Austria; available across 1 country total.

Placed on the market in Austria; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 09120120390025
Basic UDI-DI: 912012039disposalsystemYD
Reference / catalog number: HC, HP, HU
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: Sammel- und Entsorgungssystem für medizinische Spülflüssigkeiten
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A0699DRAINAGE AND FLUID COLLECTION 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

DP, DE, DU, DC912012039disposalsystemYDOn 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.