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 1–25 of 272 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
VAYA-101	`VAYA-101`	`05903111848378`	2	On the market
VAYA-102	`VAYA-102`	`05903111848385`	2	On the market
VAYA-1281-TC	`VAYA-1281-TC`	`05904473792927`	2	On the market
VAYA-8111	`VAYA-8111`	`05903111848255`	2	On the market
VAYA-8110	`VAYA-8110`	`05903111848231`	2	On the market
VAYA-8101	`VAYA-8101`	`05903111848262`	2	On the market
VAYA-8120	`VAYA-8120`	`05903111848248`	2	On the market
VAYA-1127	`VAYA-1127`	`05903111848293`	1	On the market
VAYA-1126	`VAYA-1126`	`05903111848064`	1	On the market
VAYA-1035	`VAYA-1035`	`05903111848354`	3	On the market
VAYA-1030	`VAYA-1030`	`05903111848361`	3	On the market
VAYA-1032	`VAYA-1032`	`05903111848286`	1	On the market
VAYA-1031	`VAYA-1031`	`05903111848125`	1	On the market
VAYA-00042-54G	`VAYA-00042-54G`	`05904473793504`	1	On the market
VAYA-008	`VAYA-008`	`05904473792262`	4	On the market
VAYA-3020-M-04	`VAYA-3020-M-04`	`05903111848316`	2	On the market
VAYA-3020-M-02	`VAYA-3020-M-02`	`05903111848194`	2	On the market
VAYA-006	`VAYA-006`	`05903111848057`	2	On the market
VAYA-3004	`VAYA-3004`	`05903111848101`	2	On the market
VAYA-13000-02LTCTZ	`VAYA-13000-02LTCTZ`	`05904473793313`	1	On the market
VAYA-13000-02RTCTZ	`VAYA-13000-02RTCTZ`	`05904473793306`	1	On the market
VAYA-010	`VAYA-010`	`05904473792866`	2	On the market
VAYA-F00042-06	`VAYA-F00042-06`	`05904473793382`	1	On the market
VAYA-F-00042-47	`VAYA-F-00042-47`	`05904473793405`	1	On the market
VAYA-F00042-46	`VAYA-F00042-46`	`05904473793399`	1	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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