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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

100987 — Class I MDR by Laboratoires Anios

MD Atlas
Laboratoires Anios

EUDAMED last updated this device on Feb 20, 2026

100987

359761LA01571BTSPY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Laboratoires Anios
UDI-DI code: 03597610003943
Reference / catalog number: 100987

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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

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

CW082
EUDAMED did not publish a description for this code.
CW083
EUDAMED did not publish a description for this code.
CW085
EUDAMED did not publish a description for this code.
CW089
EUDAMED did not publish a description for this code.
CW090
EUDAMED did not publish a description for this code.
CW159
EUDAMED did not publish a description for this code.
CW167
EUDAMED did not publish a description for this code.
CW171
EUDAMED did not publish a description for this code.
CW401
EUDAMED did not publish a description for this code.
CW185
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement	Sep 15, 2021	Still on market
Belgium	May 21, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03597610003943
Basic UDI-DI: 359761LA01571BTSPY
Reference / catalog number: 100987
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: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V80CLINICAL USE ACCESSORIES NOT INCLUDED IN OTHER CLASSES

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