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fără legătură salva Alerga direktiva iso medicinski pripomočki Prin lege pence bârfă

dentalni medicinski pripomoÄ ki - jazmp
dentalni medicinski pripomoÄ ki - jazmp

Machine safety and the EU Machinery Directive| TÜV SÜD | TÜV SÜD
Machine safety and the EU Machinery Directive| TÜV SÜD | TÜV SÜD

ISO 13485 - SIQ
ISO 13485 - SIQ

GROBLAR JOŽE
GROBLAR JOŽE

Sterilizacija, neviden člen zdravstva
Sterilizacija, neviden člen zdravstva

ISO 13485 - upravljanje kvalitetom za medicinske uređaje
ISO 13485 - upravljanje kvalitetom za medicinske uređaje

MDR (2017/745) - SIQ
MDR (2017/745) - SIQ

Ergonomski stol SpinaliS certifikati, patenti in nagrade
Ergonomski stol SpinaliS certifikati, patenti in nagrade

ISO 13485: Sistem vodenja kakovosti medicinskih pripomočkov
ISO 13485: Sistem vodenja kakovosti medicinskih pripomočkov

▻B IZVEDBENI SKLEP KOMISIJE (EU) 2020/439 z dne 24 marca 2020 o  harmoniziranih standardih za in vitro diagnostične medicinske
▻B IZVEDBENI SKLEP KOMISIJE (EU) 2020/439 z dne 24 marca 2020 o harmoniziranih standardih za in vitro diagnostične medicinske

Slovenian Institute for Standardization - SIST
Slovenian Institute for Standardization - SIST

Tečaj za notranje presojevalce sistema vodenja kakovosti EN ISO 13485:2016  in Uredbi (EU) 2017/745 - SIQ
Tečaj za notranje presojevalce sistema vodenja kakovosti EN ISO 13485:2016 in Uredbi (EU) 2017/745 - SIQ

Homologation and validation of automated driving functions | TÜV SÜD
Homologation and validation of automated driving functions | TÜV SÜD

MDR (2017/745) - SIQ
MDR (2017/745) - SIQ

EU: European Commission proposes formaldehyde restriction in toys | TÜV SÜD
EU: European Commission proposes formaldehyde restriction in toys | TÜV SÜD

Disposable Jelly Tab™ Sensor
Disposable Jelly Tab™ Sensor

Certificates and rewards - Office chairs Spinalis
Certificates and rewards - Office chairs Spinalis

SIQ Ljubljana Becomes a Notified Body in Accordance with the Medical Device  Regulation - SIQ
SIQ Ljubljana Becomes a Notified Body in Accordance with the Medical Device Regulation - SIQ

Certificates - magnetic therapy Biomag
Certificates - magnetic therapy Biomag

3686 / 28 / 15. 4. 2011 PRILOGA 2 Seznam standardov – Direktiva 98/79/ES  Evropskega parlamenta in Sveta z dne 27. oktobra 1998
3686 / 28 / 15. 4. 2011 PRILOGA 2 Seznam standardov – Direktiva 98/79/ES Evropskega parlamenta in Sveta z dne 27. oktobra 1998

SLOVENSKI STANDARD SIST-TP CEN/TR 17223: PDF Free Download
SLOVENSKI STANDARD SIST-TP CEN/TR 17223: PDF Free Download

IFUs for reprocessing | TÜV SÜD
IFUs for reprocessing | TÜV SÜD

SIST EN ISO 13485:2016/A11:2021 - Medical devices - Quality management  systems - Requirements for
SIST EN ISO 13485:2016/A11:2021 - Medical devices - Quality management systems - Requirements for

EN ISO 15223-1:2021 - Medical devices - Symbols to be used with information  to be supplied by the
EN ISO 15223-1:2021 - Medical devices - Symbols to be used with information to be supplied by the