Ritm Okb Zao

FDA Filings

This page includes the latest FDA filings for Ritm Okb Zao. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3007028037
• FEI Number: 3007028037
• Name: RITM OKB ZAO
• Owner & Operator: RITM OKB ZAO
• Contact Address: 99, PETROVSKAYA --; TAGANROG RU-ROS Rostovskaya oblast 347900 RU
• Official Correspondent:
  • Tatiana - Timoshenko
  • 7-8634-623179-x
• US Agent:
  • Vladimir Goncharov Phd
  • 989 2723627
  • 817 4022037
  • Vladimir.tx@gmail.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 99, PETROVSKAYA ; TAGANROG Rostovskaya oblast, 347900 RU
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K131513 | GZJ RITM OKB ZAO	SCENAR	2014-12-04
PMN K131513 | GZJ RITM OKB ZAO	SCELAP	2014-12-04
PMN K131513 | GXY RITM OKB ZAO	SCENAR	2014-12-04
PMN K131513 | GXY RITM OKB ZAO	SCELAP	2014-12-04
PMN K131513 RITM OKB ZAO	SCENAR (SCELAP, ENISAR, IPENS) CUTANEOUS ELECTRODE FAMILY	2014-07-11
PMN K092117 | GZJ RITM OKB ZAO	SCENAR	2010-10-07
PMN K092117 | GZJ RITM OKB ZAO	SCELAP	2010-10-07
PMN K092117 RITM OKB ZAO	SCENAR, MODEL 10	2010-05-28
HCC RITM OKB ZAO	SCENAR	2006-12-29
HCC RITM OKB ZAO	SCELAP	2006-12-29