Pure Global

Fluid Lens

์œ ์ˆ˜์ •์ฒด์ธ๊ณต์ˆ˜์ •์ฒด

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 No. 22-619. Approved on Sep 16, 2022. Registered by Koryo iTECH 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 Database
Powered by Pure Global AI
MFDS Official Data
Unknown
Basic Information
Item Serial Number
2022004733
License Number
No. 22-619
์ œํ—ˆ22-619ํ˜ธ
Classification Number
B04140.04
Device Class (Risk Classification)
Unknown
Classification Name
Fluid Intraocular Lens
์œ ์ˆ˜์ •์ฒด ์ธ๊ณต ์ˆ˜์ •์ฒด
Official English Name
phakic intraocular lens
Company Information
Entity Name (Company)
Koryo iTECH Co., Ltd.
(์ฃผ)๊ณ ๋ ค์•„์ดํ…
Category
Manufacturing
์ œ์กฐ์—…
Business License Number
์ œ 2667 ํ˜ธ
Important Dates & Status
Item Approval Date
Sep 16, 2022
Business Permit Date
Apr 21, 2008
Expiration Period
2022-09-16 ~ 2027-09-15
Model Information
Model Name
eyelike S-Flex
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing