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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

Profilis PaincAth — Class IIb MDR by DISTRICLASS MEDICAL SA

MD Atlas
DISTRICLASS MEDICAL SA

EUDAMED last updated this device on Oct 24, 2025

Profilis PaincAth

3665642PaincAthKC

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DISTRICLASS MEDICAL SA
UDI-DI code: 03665642300627
Reference / catalog number: P500-05R

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Manufacturer information

Organization name: DISTRICLASS MEDICAL SA
SRN: FR-MF-000001199
Manufacturer status: Active

Related devices

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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

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

CW010
EUDAMED did not publish a description for this code.
CW011
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW032
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW025
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: Profilis PaincAth
UDI-DI code: 03665642300627
Basic UDI-DI: 3665642PaincAthKC
Reference / catalog number: P500-05R
Issuing entity: GS1

Classification

Risk category: Class IIb
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: 0.5 MU50
1 MU50
500 MU50

EMDN nomenclature code(s)

A030499ADMINISTRATION KITS - 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
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Software identification