South Korea MFDS registration Reception No. 22-2193
Manual periosteal detachment
KO: 수동식골막박리기
South Korea·Class I·DSHITECH Co., Ltd.·Approved Dec 22, 2022Basic information
- Item Serial Number
- 2022006626
- License Number
- Reception No. 22-2193
- Classification Number
- A48020.01(1)
- Device Class (Risk Classification)
- Class I
- Classification Name
- Manual periosteal detachment
- Official English Name
- Dissector, periosteum, manually-operated
수신22-2193호
수동식골막박리기
Company information
- Entity Address
- 경기도 하남시 서하남로43번길 166 2층 (감북동)
- Manufacturer
- FUJITA Medical Instruments Co., Ltd.
- Category
- Import business
- Business License Number
- 제 73 호
수입업
Important dates & status
- Item Approval Date
- Dec 22, 2022
- Business Permit Date
- Sep 21, 2004
- Expiration Period
- 2022-12-22 ~ 2027-12-21
- For Export
- 아니오
Model information
- Model Name
- 8015-01 and 68 other cases
8015-01외 68건
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. 22-2193. Approved on Dec 22, 2022. Registered by DSHITECH Co., Ltd..
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