South Korea MFDS registration Reception No. 23-3
Bone forceps
KO: 골겸자
South Korea·Class I·DSHITECH Co., Ltd.·Approved Jan 02, 2023Basic information
- Item Serial Number
- 2023000005
- License Number
- Reception No. 23-3
- Classification Number
- A45020.05(1)
- Device Class (Risk Classification)
- Class I
- Classification Name
- Bone forceps
- Official English Name
- Forceps, bone
수신23-3호
골겸자
Company information
- Entity Address
- 경기도 하남시 서하남로43번길 166 2층 (감북동)
- Manufacturer
- FUJITA Medical Instrumetns Co., Ltd.
- Category
- Import business
- Business License Number
- 제 73 호
수입업
Important dates & status
- Item Approval Date
- Jan 02, 2023
- Business Permit Date
- Sep 21, 2004
- Expiration Period
- 2023-01-02 ~ 2028-01-01
- For Export
- 아니오
Model information
- Model Name
- 8211-10 and 10 other cases
8211-10외 10건
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 Reception No. 23-3. Approved on Jan 02, 2023. Registered by DSHITECH Co., Ltd..
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