Reagent kit for enzyme-linked immunosorbent assay of prgesterone in human serum (SteroidELISA-progesterone-01)
Russia·Unknown·CJSC Alkor Bio·Registered June 24, 2005·N/A- Device Name (English)
- Reagent kit for enzyme-linked immunosorbent assay of prgesterone in human serum (SteroidELISA-progesterone-01)
- Device Name (Russian)
- Набор реагентов для иммуноферментного определения пргестерона в сыворотке крови человека (СтероидИФА-прогестерон-01)
- Device Type (English)
- N/A
- Device Type (Russian)
- Unknown
- Risk Class
- N/A
- Registry Key
- o27243
- Registration Number
- ФС 012а17081836-05
- Registration Date
- June 24, 2005
- Validity Period
- June 24, 2010
- Manufacturer Name (English)
- CJSC Alkor Bio
- Manufacturer Name (Russian)
- ЗАО Алкор Био
- Country (English)
- Russia
- Country (Russian)
- Россия
- Legal Address (English)
- Saint Petersburg
- Legal Address (Russian)
- Санкт-Петербург
Access comprehensive regulatory information for Reagent kit for enzyme-linked immunosorbent assay of prgesterone in human serum (SteroidELISA-progesterone-01) in the Russia medical device market through Pure Global AI's free database. This medical device is registered under Roszdravnadzor registration number ФС 012а17081836-05 and manufactured by CJSC Alkor Bio. The device was registered on June 24, 2005.
This page provides complete registration details including device type, manufacturer information, country of origin (Russia), 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.