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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

2030462 — Class I MDR by Coopération…

MD Atlas
Coopération pharmaceutique française

EUDAMED last updated this device on Jul 29, 2025

2030462

370151010004ZB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Coopération pharmaceutique française
UDI-DI code: 03701510101634
Reference / catalog number: 2030462

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Manufacturer information

Organization name: Coopération pharmaceutique française
SRN: FR-MF-000002412
Manufacturer status: Active

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Critical warnings

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

CW999
Quel que soit le type de morsures ou piqûres venimeuses, il est primordial de garder son calme ; l’excitation accélère la diffusion du venin dans le sang et peut rendre inefficace l’utilisation de Venimex. Venimex permet d’extraire le venin d’une plaie mais ne remplace pas une prise en charge médicale. En cas de réactions allergiques, Venimex ne prévient pas l’apparition d’œdème de Quincke. Dans les cas graves, consulter rapidement un médecin.
CW999
Ne pas appliquer Venimex sur les muqueuses, paupières et parties génitales.
CW999
Attention : Venimex craint les chutes et les chocs.

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 03701510101634
Basic UDI-DI: 370151010004ZB
Reference / catalog number: 2030462
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: VENIMEX U
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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.