Pure Global

Reusable endoscope cannula

์žฌ์‚ฌ์šฉ๊ฐ€๋Šฅ ๋‚ด์‹œ๊ฒฝ ์บ๋‰ผ๋Ÿฌ

This Unknown medical device is registered with South Korea's Ministry of Food and Drug Safety (MFDS / ์‹ํ’ˆ์˜์•ฝํ’ˆ์•ˆ์ „์ฒ˜) under license number Av 23-1779. Approved on Jul 20, 2023. Registered by Medtronic 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.

Free Database
Powered by Pure Global AI
MFDS Official Data
Unknown
Basic Information
Item Serial Number
2023004255
License Number
Av 23-1779
์ˆ˜์‹ 23-1779ํ˜ธ
Classification Number
A31010.22
Device Class (Risk Classification)
Unknown
Classification Name
Reusable endoscope cannula
์žฌ์‚ฌ์šฉ๊ฐ€๋Šฅ ๋‚ด์‹œ๊ฒฝ ์บ๋‰ผ๋Ÿฌ
Official English Name
Endotherapy cannula, reusable
Company Information
Entity Name (Company)
Medtronic Korea
๋ฉ”๋“œํŠธ๋กœ๋‹‰์ฝ”๋ฆฌ์•„(์œ )
Category
Import business
์ˆ˜์ž…์—…
Business License Number
์ œ 245 ํ˜ธ
Important Dates & Status
Item Approval Date
Jul 20, 2023
Business Permit Date
Feb 01, 2005
Expiration Period
2023-07-20 ~ 2028-07-19
Model Information
Model Name
RC8STS
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing