Statistics for Arcotech Janusz Rugała S.K.A.

14Total Devices

14Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

1Countries

Certificate health for Arcotech Janusz Rugała S.K.A.

No certificates registered for this manufacturer.

Showing 1–14 of 14 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
BLF-07BKTE	`BLF-07BKTE`	`05904933523665`	1	On the market
BLF-14BKBE	`BLF-14BKBE`	`05904933523733`	1	On the market
BLF-15BK	`BLF-15BK`	`05904933523740`	1	On the market
BLF-16BE	`BLF-16BE`	`05904933523757`	1	On the market
BLF-17BKBE	`BLF-17BKBE`	`05904933523764`	1	On the market
BLF-17BK	`BLF-17BK`	`05904933523771`	1	On the market
BLF-18	`BLF-18`	`05904933523788`	1	On the market
BLM-02B	`BLM-02B`	`05904933524143`	1	On the market
BLM-03B	`BLM-03B`	`05904933524129`	1	On the market
BLM-01W	`BLM-01W`	`05904933524136`	1	On the market
BLF-19BE	`BLF-19BE`	`05904933523795`	1	On the market
BLF-03	`BLF-03`	`05904933523610`	1	On the market
BLF-20BK	`BLF-20BK`	`05904933523801`	1	On the market
BLF-21BKBE	`BLF-21BKBE`	`05904933523818`	1	On the market

Devices placed in 1 country

EUDAMED update: Jan 14, 2025

PL-MF-000044298

Active

ZABIEGAŁA Aneta
(a) the conformity of the devices in accordance with the quality management system, before a device is released; (b) the technical documentation and the EU declaration of conformity; (c) the post-market surveillance obligations in accordance with Article 10(10) of 2017/745; (d) reporting obligations referred to in Articles 87 to 91 of 2017/745; (e) issuing statement referred to in Section 4.1 of Chapter II of Annex XV of 2017/745
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