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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

67966 — IVDR Class A IVDR by Aidian Oy

MD Atlas
Aidian Oy

EUDAMED last updated this device on May 18, 2022

67966

6438115QRPlungersA7

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Aidian Oy
UDI-DI code: 06438115001188
Reference / catalog number: 67966

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Manufacturer information

Organization name: Aidian Oy
SRN: FI-MF-000023611
Manufacturer status: Active

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154980B-06438115001652On the market 67748B-06438115000648On the market 67265B-06438115000488On the market 67249B-06438115000471On the market 67839B-06438115000587On the market

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.

CW009
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Finland; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 06438115001188
Basic UDI-DI: 6438115QRPlungersA7
Reference / catalog number: 67966
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 50
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0501010280CAPILLARY BLOOD COLLECTION DEVICES - ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
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Software identification