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Organization name
UDI-DI code
Reference / catalog number

1343408DF — Class IIb MDD by Laboratoires Anios

MD Atlas
Laboratoires Anios

EUDAMED last updated this device on Apr 30, 2026

1343408DF

B-03597610646980

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Laboratoires Anios
UDI-DI code: 03597610646980
Reference / catalog number: 1343408DF

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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

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

CW081
EUDAMED did not publish a description for this code.
CW106
EUDAMED did not publish a description for this code.
CW139
EUDAMED did not publish a description for this code.
CW159
EUDAMED did not publish a description for this code.
CW166
EUDAMED did not publish a description for this code.
CW167
EUDAMED did not publish a description for this code.
CW177
EUDAMED did not publish a description for this code.
CW430
EUDAMED did not publish a description for this code.
CW444
EUDAMED did not publish a description for this code.
CW179
EUDAMED did not publish a description for this code.
CW397
EUDAMED did not publish a description for this code.
CW416
EUDAMED did not publish a description for this code.
CW062
EUDAMED did not publish a description for this code.
CW073
EUDAMED did not publish a description for this code.
CW076
EUDAMED did not publish a description for this code.
CW080
EUDAMED did not publish a description for this code.
CW119
EUDAMED did not publish a description for this code.
CW150
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	May 21, 2010	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03597610646980
Basic UDI-DI: B-03597610646980
Reference / catalog number: 1343408DF
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)

D050101PERACETIC AND ACETIC ACID WITH HYDROGEN PEROXIDE 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
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Software identification