Cardioblate CryoFlex surgical ablation system consisting of:- Cardioblate CryoFlex surgical ablation console.1. Probe for surgical ablation Cardioblate CryoFlex variants:- Probe for surgical ablation Cardioblate CryoFlex length 10 cm in the composition:- Probe for... (see the full description in the card)
Russia·Unknown·Medtronic Inc.·Registered June 13, 2018·Class 3- Device Name (English)
- Cardioblate CryoFlex surgical ablation system consisting of:- Cardioblate CryoFlex surgical ablation console.1. Probe for surgical ablation Cardioblate CryoFlex variants:- Probe for surgical ablation Cardioblate CryoFlex length 10 cm in the composition:- Probe for... (see the full description in the card)
- Device Name (Russian)
- Система для хирургической абляции Cardioblate CryoFlex в составе:- Консоль для хирургической абляции Cardioblate CryoFlex.1. Зонд для хирургической абляции Cardioblate CryoFlex варианты исполнения:- Зонд для хирургической абляции Cardioblate CryoFlex длина 10 см в составе:- Зонд для... (см. в карточке полное описание)
- Device Type (English)
- N/A
- Device Type (Russian)
- Unknown
- Risk Class
- Class 3
- OKPD Code
- 32.50.50.000
- Registry Key
- 28838
- Registration Number
- РЗН 2016/4446
- Registration Date
- June 13, 2018
- Validity Period
- January 01, 2262
- Manufacturer Name (English)
- Medtronic Inc.
- Manufacturer Name (Russian)
- Медтроник Инк.
- Country (English)
- USA
- Country (Russian)
- USA
- Legal Address (English)
- США Medtronic Inc. 710 Medtronic Parkway Minneapolis MN 55432 USA
- Legal Address (Russian)
- США Medtronic Inc. 710 Medtronic Parkway Minneapolis MN 55432 USA
- Manufacturing Address
- Medtronic Inc. 3800 Annapolis Lane Minneapolis MN 55447 USA
Access comprehensive regulatory information for Cardioblate CryoFlex surgical ablation system consisting of:- Cardioblate CryoFlex surgical ablation console.1. Probe for surgical ablation Cardioblate CryoFlex variants:- Probe for surgical ablation Cardioblate CryoFlex length 10 cm in the composition:- Probe for... (see the full description in the card) in the Russia medical device market through Pure Global AI's free database. This Class 3 medical device is registered under Roszdravnadzor registration number РЗН 2016/4446 and manufactured by Medtronic Inc.. The device was registered on June 13, 2018.
This page provides complete registration details including device type, manufacturer information, country of origin (USA), and regulatory compliance data from the official Russia Roszdravnadzor medical device database. Pure Global AI offers free access to Russia's complete medical device registry, helping global MedTech companies navigate Roszdravnadzor regulations efficiently.