Statistics for STERIWUND spol. s r.o.

554Total Devices

52Basic UDI-DIs

0Not destined for EU market

1Certificates

1Valid

0Expiring < 6 months

2Countries

Certificate health for STERIWUND spol. s r.o.

Showing 126–150 of 554 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
Gauze ball non-sterile	`0736`	`08595154104879`	200	On the market
Gauze ball non-sterile	`0734`	`08595154104374`	100	On the market
Gauze ball non-sterile	`1054`	`08595154104398`	50	On the market
Gauze ball non-sterile	`0737`	`08595154104367`	100	On the market
Gauze ball non-sterile	`0733`	`08595154106323`	200	On the market
Gauze swab non-sterile	`0176MN`	`08595154101434`	100	On the market
Gauze swab non-sterile	`0178MN`	`08595154101182`	100	On the market
Gauze swab non-sterile	`0175MN`	`08595154101243`	100	On the market
Gauze swab non-sterile	`0177MN`	`08595154101342`	100	On the market
Gauze swab, sterile	`0102`	`08595154101021`	1	On the market
Gauze swab, sterile	`0609`	`08595154101694`	2	On the market
Gauze swab, sterile	`0621`	`08595154101083`	10	On the market
Gauze swab, sterile	`0619`	`08595154101540`	3	On the market
Gauze swab, sterile	`0637`	`08595154102974`	3	On the market
Gauze swab, sterile	`0626`	`08595154101595`	10	On the market
Gauze swab, sterile	`0164`	`08595154101946`	4	On the market
Gauze swab, sterile	`0615`	`08595154101519`	5	On the market
Gauze swab, sterile	`0168`	`08595154101663`	4	On the market
Gauze swab, sterile	`0620`	`08595154101670`	5	On the market
Gauze swab, sterile	`0109`	`08595154101731`	1	On the market
Gauze swab, sterile	`0627`	`08595154101601`	20	On the market
Gauze swab, sterile	`0611`	`08595154101687`	5	On the market
Gauze swab, sterile	`0625`	`08595154101458`	5	On the market
Gauze swab, sterile	`0614`	`08595154101793`	2	On the market
Gauze swab, sterile	`0624`	`08595154101571`	3	On the market

Devices placed in 2 countries

EUDAMED update: Feb 17, 2025

CZ-MF-000036963

Active

JAROŠOVÁ Helena
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.
Hidden