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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

Gant Latex Large 8/9 - Boite x100 — Class I MDR by CA Diffusion

MD Atlas
CA Diffusion

EUDAMED last updated this device on Nov 4, 2025

Gant Latex Large 8/9 - Boite x100

376006117GANTLATEXPVV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CA Diffusion
UDI-DI code: 03760061170148
Reference / catalog number: GLL

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Manufacturer information

Organization name: CA Diffusion
SRN: FR-MF-000012222
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

1 warning recorded — scroll inside the panel to see all entries.

CW083
Natural rubber latex (from Hevea brasiliensis sap) contains allergenic proteins. These proteins can trigger: Contact skin reactions (eczema, itching, redness), Or immediate type I allergic reactions (more severe: urticaria, edema, asthma, or even anaphylactic shock).

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: Gant Latex Large 8/9 - Boite x100
UDI-DI code: 03760061170148
Basic UDI-DI: 376006117GANTLATEXPVV
Reference / catalog number: GLL
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: Gant d'examen en latex poudrés, non stériles - taille large. Boîte de 100 gants.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T01010101POWDERED LATEX SURGICAL GLOVES

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

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Expiration date
Manufacturing date
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Software identification