RoboMapСтандарты робототехники
документов: 25
Соответствие стандарту - это документ, а не свойство робота. Справочник показывает сертификат там, где он назван источником, и молчит там, где его нет.
- Boston Dynamics Spot EU Declaration of Conformity v4 (2024-01-09)
- CE marking of Carti Low-Profile (option)
- CE-MD certification of AGIBOT A2 Ultra
- CE-RED certification of AGIBOT A2 Ultra
- CR certification of AGIBOT A2 Ultra
- EN ISO 10218-1:2011
- FCC certification of AGIBOT A2 Ultra
- FDA 510(k) K050369 INTUITIVE SURGICAL DA VINCI SURGICAL SYSTEM, MODEL IS2000 (decision 2005-04-29)
- FDA 510(k) K081137 INTUITIVE SURGICAL DA VINCI SI SURGICAL SYSTEM: MODEL IS3000 (decision 2009-02-18)
- FDA 510(k) K131861 DA VINCI SURGICAL SYSTEM, ENDOWRIST INSTRUMENTS AND ACCESSORIES (decision 2014-03-28)
- FDA 510(k) K131962 DA VINCI SP SURGICAL SYSTEM, ENDOWRIST SP INSTRUMENTS, AND ACCESSORIES (decision 2014-04-17)
- FDA 510(k) K171294 da Vinci X Surgical System (decision 2017-05-26)
- FDA 510(k) K173906 da Vinci SP Surgical System, EndoWrist SP Instruments, and Accessories (decision 2018-05-31)
- FDA 510(k) K182188 Ion Endoluminal System ; Flexision Biopsy Needle (decision 2019-02-14)
- FDA 510(k) K200574 EksoNR (letter 2020-06-15)
- FDA 510(k) K232610 da Vinci Surgical System Model IS5000, da Vinci Insufflator and Tube Set with Smoke Evacuation (decision 2024-03-14)
- FDA 510(k) K250904 Atalante X (letter 2025-10-24)
- FDA 510(k) K252045 Ion Endoluminal System (IF1000) (decision 2025-09-23)
- FDA 510(k) K253702 Intuitive Endoluminal Gastrointestinal System (IG1000) (decision 2026-08-07)
- FDA 510(k) K261824 da Vinci Surgical System, Model IS5000 (decision 2026-07-31)
- ISO 8373:2012
- ISO 8373:2021
- NSF certification of Servi and Servi Plus
- Robotiq Vision System Declaration of Incorporation (translation), November 2017
- TÜV NORD certificate 44 780 14097607 (EN ISO 10218-1:2011)