A set of reagents for the bacteriological analyzer of the BACTEC 9000 series (see Appendix on 1 sheet) 1. Aerobic Culture Media [BD BACTEC TM PLUS + Aerobic/F] 2. Anaerobic Culture Media [BD BACTEC TM PLUS + Anaerobic/F] 3. Medium for the cultivation of aerobes from infant blood samples [BD BACTEC TM PEDS PLUS TM /F ] 4. Mushroom Culture Media [BD BACTEC TM Mycosis-IC/F] 5.Lysis Anaerobes Culture Media [BD BACTEC TM Lytic/10 Anaerobic/F] 6.Mycobacterial Yeast Fungal Culture Media [BD BACTEC TM MYCO/F Lytic] 7. Nutritional additive to BACTEC media [BD BACTEC TM FOS TM Kit] 8. Adult Blood Collection Kit [ Safety-Lok TM Blood Collection Set (Adult)] 9. Device for blood collection in children [ Safety-Lok TM Blood Collection Set (Pediatrict)] 10. Direct Draw Adapter for BACTEC TM 9000 bottles 11. Set for reseeding cultures from BACTEC vials [ BD BACTEC TM Subculturing Unit] - Roszdravnadzor Registration МЗ РФ № 2003/1408

Access comprehensive regulatory information for A set of reagents for the bacteriological analyzer of the BACTEC 9000 series (see Appendix on 1 sheet) 1. Aerobic Culture Media [BD BACTEC TM PLUS + Aerobic/F] 2. Anaerobic Culture Media [BD BACTEC TM PLUS + Anaerobic/F] 3. Medium for the cultivation of aerobes from infant blood samples [BD BACTEC TM PEDS PLUS TM /F ] 4. Mushroom Culture Media [BD BACTEC TM Mycosis-IC/F] 5.Lysis Anaerobes Culture Media [BD BACTEC TM Lytic/10 Anaerobic/F] 6.Mycobacterial Yeast Fungal Culture Media [BD BACTEC TM MYCO/F Lytic] 7. Nutritional additive to BACTEC media [BD BACTEC TM FOS TM Kit] 8. Adult Blood Collection Kit [ Safety-Lok TM Blood Collection Set (Adult)] 9. Device for blood collection in children [ Safety-Lok TM Blood Collection Set (Pediatrict)] 10. Direct Draw Adapter for BACTEC TM 9000 bottles 11. Set for reseeding cultures from BACTEC vials [ BD BACTEC TM Subculturing Unit] in the Russia medical device market through Pure Global AI's free database. This medical device is registered under Roszdravnadzor registration number МЗ РФ № 2003/1408 and manufactured by Becton Dickinson. The device was registered on October 28, 2003.

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.