South Korea MFDS registration In Vitro Reception No. 18-1382
Sample processing equipment
KO: 표본가공장치
South Korea·Class I·Agilent Technologies Korea·Approved Jul 05, 2018Basic information
- Item Serial Number
- 2018003775
- License Number
- In Vitro Reception No. 18-1382
- Classification Number
- I02010.01(1)
- Device Class (Risk Classification)
- Class I
- Classification Name
- Sample processing equipment
- Official English Name
- Sample processing instruments
체외수신18-1382호
표본가공장치
Company information
- Entity Address
- 서울특별시 서초구 강남대로 369 , 13층, 14층
- Manufacturer
- Leica Biosystems Richmond
- Category
- Import business
- Business License Number
- 체외 제 1907 호
수입업
Important dates & status
- Item Approval Date
- Jul 05, 2018
- Business Permit Date
- Jan 18, 2010
- Expiration Period
- 2020-10-08 ~ 2030-06-30
- For Export
- 아니오
Model information
- Model Name
- Hybridizer, S2451
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. 18-1382. Approved on Jul 05, 2018. Registered by Agilent Technologies Korea.
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