Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

3104 — Class IIa MDR by ALPRO MEDICAL GMBH

MD Atlas
ALPRO MEDICAL GMBH

EUDAMED last updated this device on May 12, 2026

3104

++E251000508008Q

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ALPRO MEDICAL GMBH
UDI-DI code: +E25131041
Reference / catalog number: 3104

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

Related devices

8750++E25101875000D2On the market ALPRO-BCS pressure bottle++E25101877500E9On the market 3123++E251000805009AOn the market AlproJet MixCup with double adapter++E25101308500A2On the market 3193++E251000508008QOn 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.

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].
CW166
EUDAMED did not publish a description for this code.
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.

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: +E25131041
Basic UDI-DI: ++E251000508008Q
Reference / catalog number: 3104
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