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pnBAS EN ISO 18113-2:2025
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 18113-3:2025
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 18113-4:2025
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 18113-5:2025
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 20916:2025
In vitro diagnostic medical devices - Clinical performance studies using specimens from human subjects - Good study practice
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 23500-1:2025
Preparation and quality management of fluids for haemodialysis and related therapies - Part 1: General requirements
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 23500-2:2025
Preparation and quality management of fluids for haemodialysis and related therapies - Part 2: Water treatment equipment for haemodialysis applications and related therapies
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 23500-3:2025
Preparation and quality management of fluids for haemodialysis and related therapies - Part 3: Water for haemodialysis and related therapies
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 23500-4:2025
Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 23500-5:2025
Preparation and quality management of fluids for haemodialysis and related therapies - Part 5: Quality of dialysis fluid for haemodialysis and related therapies
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 5362:2025
Anaesthetic and respiratory equipment - Anaesthetic reservoir bags
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 7199:2025
Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators)
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 7921:2025
Ophthalmic optics and instruments - Near reading charts
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 80369-2:2025
Small-bore connectors for liquids and gases in healthcare applications - Part 2: Connectors for respiratory applications
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 80601-2-12:2025
Medical electrical equipment - Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 80601-2-55/A1:2025
Medical electrical equipment - Part 2-55: Particular requirements for the basic safety and essential performance of respiratory gas monitors - Amendment 1
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 80601-2-79:2025
Medical electrical equipment - Part 2-79: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 81060-2/A2:2025
Non-invasive sphygmomanometers - Part 2: Clinical investigation of intermittent automated measurement type - Amendment 2
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 8362-2:2025
Injection containers and accessories - Part 2: Closures for injection vials
30.20BAS/TC 2526.03.202507.04.2025
pnBAS EN ISO 8637-2:2025
Extracorporeal systems for blood purification - Part 2: Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
30.20BAS/TC 2526.03.202507.04.2025