Pure Global

Reusable endoscope forceps

์žฌ์‚ฌ์šฉ๊ฐ€๋Šฅ ๋‚ด์‹œ๊ฒฝ ๊ฒธ์ž

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 23-2789. Approved on Dec 04, 2023. Registered by Sekwang Corporation.

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
2023006820
License Number
Av 23-2789
์ˆ˜์‹ 23-2789ํ˜ธ
Classification Number
A31010.29
Device Class (Risk Classification)
Unknown
Classification Name
Reusable endoscope forceps
์žฌ์‚ฌ์šฉ๊ฐ€๋Šฅ ๋‚ด์‹œ๊ฒฝ ๊ฒธ์ž
Official English Name
Endotherapy forceps, reusable
Company Information
Entity Name (Company)
Sekwang Corporation
์„ธ๊ด‘์ƒ์‚ฌ
Category
Import business
์ˆ˜์ž…์—…
Business License Number
์ œ 35 ํ˜ธ
Important Dates & Status
Item Approval Date
Dec 04, 2023
Business Permit Date
Aug 19, 2004
Expiration Period
2023-12-04 ~ 2028-12-03
Model Information
Model Name
S401-279.1S
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing