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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

8001752 — Class IIa MDD by Applimed SA

MD Atlas
Applimed SA

EUDAMED last updated this device on Sep 2, 2025

8001752

B-07640178430198

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Applimed SA
UDI-DI code: 07640178430198
Reference / catalog number: 8001752

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Manufacturer information

Organization name: Applimed SA
SRN: CH-MF-000046641
Manufacturer status: Active

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Critical warnings

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

CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW156
Do not bend the cannula; Do not use the device as a rubbing ustensil against tissues or bones; Make sure other mechanical devices do not come into contact with the cannula

Market distribution

Primary placement in Czechia; available across 2 countries total.

Country	On market since	Until
CzechiaPrimary placement		Still on market
France		Still on market

Device identification

Trade name: not provided
UDI-DI code: 07640178430198
Basic UDI-DI: B-07640178430198
Reference / catalog number: 8001752
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: 1 Aiguille boutonnée soudage laser 80mm 14.5G, métal 100 Peelpacks/boîte 10 Boîtes/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)

A06010103CANNULAS AND TIPS FOR ASPIRATION AND IRRIGATION, 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
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.