Pure Global

Flow cytometry device

์œ ์„ธํฌ๋ถ„์„์žฅ์น˜

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 In Vitro Reception No. 22-1387. Approved on Aug 11, 2022. Registered by Beckman Coulter 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
2022004127
License Number
In Vitro Reception No. 22-1387
์ฒด์™ธ์ˆ˜์‹ 22-1387ํ˜ธ
Classification Number
K01060.01
Device Class (Risk Classification)
Unknown
Classification Name
Flow cytometry device
์œ ์„ธํฌ๋ถ„์„์žฅ์น˜
Official English Name
Flow cytometry
Company Information
Entity Name (Company)
Beckman Coulter Korea
ํ•œ๊ตญ๋ฒกํฌ๋งŒ์ฟจํ„ฐ(์ฃผ)
Category
In vitro diagnostic import business
์ฒด์™ธ์ง„๋‹จ์ˆ˜์ž…์—…
Business License Number
์ฒด์™ธ ์ œ 1783 ํ˜ธ
Important Dates & Status
Item Approval Date
Aug 11, 2022
Business Permit Date
Mar 20, 2009
Expiration Period
2022-08-11 ~ 2027-08-10
Model Information
Model Name
Navios EX Flow Cytometer
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing