South Korea MFDS registration In Vitro Reception No. 22-1649
Automatic Blood Count
KO: 자동혈구계산기
Basic information
- Item Serial Number
- 2022004927
- License Number
- In Vitro Reception No. 22-1649
- Classification Number
- J03020.01(1)
- Device Class (Risk Classification)
- Class I
- Classification Name
- Automatic Blood Count
- Official English Name
- Hematology analyzer, cell-quantifying
체외수신22-1649호
자동혈구계산기
Company information
- Entity Address
- 서울특별시 강남구 영동대로 421 7층 (대치동, 삼탄빌딩)
- Manufacturer
- CellaVision AB
- Category
- Import business
- Business License Number
- 체외 제 371 호
수입업
Important dates & status
- Item Approval Date
- Sep 28, 2022
- Business Permit Date
- Mar 30, 2005
- Expiration Period
- 2022-09-28 ~ 2027-09-27
- For Export
- 아니오
Model information
- Model Name
- DM9600
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. 22-1649. Approved on Sep 28, 2022. Registered by Abbott 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.
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