Statistics for Vaya sp. z o.o.

272Total Devices

11Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

1Countries

Certificate health for Vaya sp. z o.o.

No certificates registered for this manufacturer.

Showing 26–50 of 272 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
VAYA-1320	`VAYA-1320`	`05903111848187`	1	On the market
VAYA-1317	`VAYA-1317`	`05903111848118`	1	On the market
VAYA-1000	`VAYA-1000`	`05903111848156`	1	On the market
VAYA-1076	`VAYA-1076`	`05903111848224`	1	On the market
VAYA-1075	`VAYA-1075`	`05903111848217`	1	On the market
VAYA-1051	`VAYA-1051`	`05904473792910`	1	On the market
VAYA-1050	`VAYA-1050`	`05904473792903`	1	On the market
VAYA-009	`VAYA-009`	`05904473792422`	6	On the market
VAYA-007	`VAYA-007`	`05903111848279`	9	On the market
VAYA-1014-M03	`VAYA-1014-M03`	`05904473792897`	1	On the market
VAYA-1014-M02	`VAYA-1014-M02`	`05904473792880`	1	On the market
VAYA-1040-04	`VAYA-1040-04`	`05903111848170`	1	On the market
VAYA-1040-02	`VAYA-1040-02`	`05903111848132`	1	On the market
VAYA-F-00043-07	`VAYA-F-00043-07`	`05904473793429`	2	On the market
VAYA-F-00043-12	`VAYA-F-00043-12`	`05904473793443`	2	On the market
VAYA-F-00043-06	`VAYA-F-00043-06`	`05904473793412`	2	On the market
VAYA-1100	`VAYA-1100`	`05903111848088`	3	On the market
VAYA-1106	`VAYA-1106`	`05904473792941`	1	On the market
VAYA-1105	`VAYA-1105`	`05903111848071`	1	On the market
VAYA-F-00043-11	`VAYA-F-00043-11`	`05904473793436`	2	On the market
VAYA-1038	`VAYA-1038`	`05903111848149`	1	On the market
VAYA-MC-CLIP-10	`VAYA-MC-CLIP-10`	`05904473793511`	10	On the market
VAYA-MC-CLIP-100	`VAYA-MC-CLIP-100`	`05904473793542`	100	On the market
VAYA-MC-CLIP-25	`VAYA-MC-CLIP-25`	`05904473793528`	25	On the market
VAYA-MC-CLIP-50	`VAYA-MC-CLIP-50`	`05904473793535`	50	On the market

Devices placed in 1 country

MD Atlas update: May 27, 2026

PL-MF-000034726

Active

SIERPINSKI Grzegorz
- verification of the compliance of medical devices with the requirements of the Medical Devices Regulation and Quality Management System, - preparation of and updating the technical documentation and compliance declarations, - participation in the mandatory supervision of the product, after introducing it to the market, - registration of the products, - reporting of the incidents and complying with the related procedures
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