South Korea MFDS registration In Vitro Reception No. 18-895
Cell and tissue staining reagent I
KO: 세포및조직염색시약I
Basic information
- Item Serial Number
- 2018002404
- License Number
- In Vitro Reception No. 18-895
- Classification Number
- O02010.01(1)
- Device Class (Risk Classification)
- Class I
- Classification Name
- Cell and tissue staining reagent I
- Official English Name
- Histological staining reagent Ⅰ
체외수신18-895호
세포및조직염색시약I
Company information
- Entity Address
- 서울특별시 서초구 강남대로 369 , 13층, 14층
- Manufacturer
- Agilent Technologies Denmark ApS
- Category
- Import business
- Business License Number
- 체외 제 1907 호
수입업
Important dates & status
- Item Approval Date
- Apr 27, 2018
- Business Permit Date
- Jan 18, 2010
- Expiration Period
- 2020-10-08 ~ 2030-05-31
- For Export
- 아니오
Model information
- Model Name
- EnVision FLEX HRP Magenta, High pH (Dako Omnis), GV900
About this record
This Class I medical device is registered with South Korea's Ministry of Food and Drug Safety (MFDS / 식품의약품안전처) under license number In Vitro Reception No. 18-895. Approved on Apr 27, 2018. Registered by Agilent Technologies Korea.
Pure Global AI provides free access to comprehensive South Korea MFDS registration data, helping global MedTech companies analyze market presence and regulatory compliance for medical devices in South Korea.
Free DatabasePowered by Pure Global AIMFDS Official DataClass I