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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

8600026 — Class IIa MDR by ALPRO MEDICAL GMBH

MD Atlas
ALPRO MEDICAL GMBH

EUDAMED last updated this device on May 12, 2026

8600026

++E251002001006Q

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ALPRO MEDICAL GMBH
UDI-DI code: +E25186000261
Reference / catalog number: 8600026

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Manufacturer information

Organization name: ALPRO MEDICAL GMBH
SRN: DE-MF-000010603
Manufacturer status: Active

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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.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Dec 31, 2028	Still on market

Device identification

Trade name: not provided
UDI-DI code: +E25186000261
Basic UDI-DI: ++E251002001006Q
Reference / catalog number: 8600026
Issuing entity: HIBCC

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: Ready-to-use solution for the disinfection of medical and dental unit waterlines and for the prevention of biofilm formation.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

D0299BIGUANIDES FOR THE DISINFECTION OF MEDICAL 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

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Software identification