South Korea MFDS registration Suhe 23-383
Electrocorporeal shock fracture crusher
KO: 전기체외충격파쇄석기
South Korea·Unknown·Dong Aesti Co., Ltd.·Approved Dec 01, 2023Basic information
- Item Serial Number
- 2023006814
- License Number
- Suhe 23-383
- Classification Number
- A18010.02
- Device Class (Risk Classification)
- Unknown
- Classification Name
- Electric Extracorporeal Shock Wave Crusher
- Official English Name
- Lithotriptor, external, electromechanical
수허23-383호
전기 체외충격파 쇄석기
Company information
- Category
- Import business
- Business License Number
- 제 561 호
수입업
Important dates & status
- Item Approval Date
- Dec 01, 2023
- Business Permit Date
- May 16, 2005
- Expiration Period
- 2023-12-01 ~ 2028-11-30
Model information
- Model Name
- MODULITH® SLX-F2 FD21
About this record
This Unknown medical device is registered with South Korea's Ministry of Food and Drug Safety (MFDS / 식품의약품안전처) under license number Suhe 23-383. Approved on Dec 01, 2023. Registered by Dong Aesti Co., Ltd..
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 DataUnknown