Statistics for MAJOR CZ s.r.o.

896Total Devices

896Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

1Countries

Certificate health for MAJOR CZ s.r.o.

No certificates registered for this manufacturer.

Showing 876–896 of 896 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV56D2VKW`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV56D3VKZ`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV59C3VLH`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FDV00A3VED`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV59D3VLN`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV48A3VKM`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV53B1VJU`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV49D2VL8`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV49A2VKR`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV50C2VJF`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV30C4VHX`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV40D2VJ9`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV30B3VHP`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV44C4VK6`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV17B1VJC`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV17C3VJP`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV22D3VJ4`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV20A1VGZ`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV20D2VHK`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV25C1VJE`	1	On the market
MAJOR SUPER LUX VITA	`N/A`	`D-CZMF000037078FHV27B1VJP`	1	On the market

Devices placed in 1 country

MD Atlas update: May 28, 2026

CZ-MF-000037078

Active

KNOS Svatopluk
the conformity of the MDs is appropriately checked, in accordance with the QMS under which the MDs are manufactured, before an MD is released; the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; the PMS obligations are complied with in accordance with Art.10(10) MDR; the reporting obligations referred to in Art.87–91 MDR are fulfilled; in the case of investigational MDs, the statement referred to in Section 4.1 of Annex XV MDR is issued.
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