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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

010005 — Class IIa MDR by ALPRO MEDICAL GMBH

MD Atlas
ALPRO MEDICAL GMBH

EUDAMED last updated this device on May 8, 2026

010005

++E251000508008Q

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ALPRO MEDICAL GMBH
UDI-DI code: +E2510100051
Reference / catalog number: 010005

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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.

Critical warnings

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

CW073
EUDAMED did not publish a description for this code.
CW081
EUDAMED did not publish a description for this code.
CW106
EUDAMED did not publish a description for this code.
CW158
Do not breathe gas/mist/vapours/spray.
CW167
EUDAMED did not publish a description for this code.
CW444
IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water [or shower].
CW416
IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
CW999
Immediately call a POISON CENTER/ doctor.
CW166
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	Dec 31, 2028	Still on market

Device identification

Trade name: not provided
UDI-DI code: +E2510100051
Basic UDI-DI: ++E251000508008Q
Reference / catalog number: 010005
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: Liquid concentrate for the daily disinfection and cleaning of dental suction systems with and without amalgam separator.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

D99DISINFECTANTS, ANTISEPTICS, STERILISING AGENTS AND DETERGENTS FOR 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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification