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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

4909955 — Class I MDD by Applimed SA

MD Atlas
Applimed SA

EUDAMED last updated this device on Sep 2, 2025

4909955

B-07640178430303

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Applimed SA
UDI-DI code: 07640178430303
Reference / catalog number: 4909955

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Manufacturer information

Organization name: Applimed SA
SRN: CH-MF-000046641
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.

Market distribution

Primary placement in Romania; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 07640178430303
Basic UDI-DI: B-07640178430303
Reference / catalog number: 4909955
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Set Soin 1 SF7505A, blister rigide 6 Boules tissées Ø2.5-3cm 1 Pincette 13cm, bleue 1 Pincette 13cm, verte enveloppé dans : 1 Champ 50x50cm 35 Sets/carton
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V9012NON-SPECIALIST SURGICAL INSTRUMENTS AND KITS, SINGLE-USE

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