Окклюдеры сердечные с принадлежностями: окклюдер Figulla Flex II PFO:

Land: Hviderusland

Sprog: russisk

Kilde: Министерством здравоохранения Республики (Центр экспертиз и испытаний в здравоохранении)

Produktets egenskaber Produktets egenskaber (SPC)
10-02-2021

Tilgængelig fra:

Occlutech GmbH, ГЕРМАНИЯ

Klasse:

изделия медицинского назначения

Fremstillet af:

Occlutech GmbH

Autorisation dato:

2021-02-16

Produktets egenskaber

                                INSTRUCTIONS FOR USE
FIGULLA
® FLEX II ASD OCCLUDER
116
OCCLUTECH GMBH
WINZERLAER STRASSE 2 07745 JENA, GERMANY
NOTIFIED BODY NUMBER: CE 0124
FOR CONTACT AND ADDITIONAL
PRODUCT INFORMATION, PLEASE
VISIT WWW.OCCLUTECH.COM
ISSUE DATE: REV. 01, 2018-10-11
REV: P17F03.029.01
168877_300,5x210_EJ_FSC.indd 1
2018-10-11 08:24:02
INSTRUCTIONS FOR USE
FIGULLA
® FLEX II ASD OCCLUDER
116
OCCLUTECH GMBH
WINZERLAER STRASSE 2 07745 JENA, GERMANY
NOTIFIED BODY NUMBER: CE 0124
FOR CONTACT AND ADDITIONAL
PRODUCT INFORMATION, PLEASE
VISIT WWW.OCCLUTECH.COM
ISSUE DATE: REV. 01, 2018-10-11
REV: P17F03.029.01
168877_300,5x210_EJ_FSC.indd 1
2018-10-11 08:24:02
2
ENGLISH
...............................................................................................
3
DEUTSCH
............................................................................................
17
ESPAÑOL
............................................................................................
31
FRENCH
..............................................................................................
45
ITALIANO
.............................................................................................
59
POLSKI
................................................................................................
73
PORTUGUÊS
.........................................................................................
88
TÜRKÇE
............................................................................................
102
3
English
TABLE OF CONTENTS
1.
Product description
...........................................................................................................................
3
2.
Indication for Use and Area of Application
......................................................................................
4
3.
Contraindications
..............................................................................................................................
4
4.
Warnings
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