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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

2416097FG — Class IIb MDD by Laboratoires Anios

MD Atlas
Laboratoires Anios

EUDAMED last updated this device on May 7, 2025

2416097FG

B-03597610429651

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Laboratoires Anios
UDI-DI code: 03597610429651
Reference / catalog number: 2416097FG

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Manufacturer information

Organization name: Laboratoires Anios
SRN: FR-MF-000011756
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

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

CW082
Causes skin irritation.
CW084
Causes serious eye damage.
CW104
Very toxic to aquatic life.
CW166
Avoid release to the environment
CW167
Wear protective gloves/ eye protection/ face protection.
CW397
Remove contact lenses, if present and easy to do. Continue rinsing.
CW416
Rinse cautiously with water for several minutes
CW179
Immediately call a POISON CENTER/doctor.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Apr 16, 2014	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03597610429651
Basic UDI-DI: B-03597610429651
Reference / catalog number: 2416097FG
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

D0901AMMONIUM SALTS FOR THE DISINFECTION OF MEDICAL DEVICES

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