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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

AT030711 — Class I MDR by AQUATOOLS

MD Atlas
AQUATOOLS

EUDAMED last updated this device on May 13, 2026

AT030711

376027973FILTRAY2.5GS47

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: AQUATOOLS
UDI-DI code: 03760279730004
Reference / catalog number: AT030711

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Manufacturer information

Organization name: AQUATOOLS
SRN: FR-MF-000028808
Manufacturer status: Active

Related devices

FILTRAY376027973FILTRAY2.5GS47On the market FILTRAY376027973FILTRAY2.5GS47On the market FILTRAY376027973FILTRAY2.5GS47On the market FILTRAY376027973FILTRAY2.5GS47On the market FILTRAY376027973FILTRAY2.5GS47On the market

Critical warnings

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

CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03760279730004
Basic UDI-DI: 376027973FILTRAY2.5GS47
Reference / catalog number: AT030711
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: —
Additional information URL: https://www.aqua-tools.com/our-services/technical-and-scientific-support/installation-guides
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A0499SOLUTION FILTERS - 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

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.