Pure Global

Reusable medical forceps

์žฌ์‚ฌ์šฉ๊ฐ€๋Šฅ์˜๋ฃŒ์šฉ๊ฒธ์ž

This Class I medical device is registered with South Korea's Ministry of Food and Drug Safety (MFDS / ์‹ํ’ˆ์˜์•ฝํ’ˆ์•ˆ์ „์ฒ˜) under license number Reception No. 22-461. Approved on Mar 18, 2022. Registered by Sungwoo Medical 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
Class I
Basic Information
Item Serial Number
2022001375
License Number
Reception No. 22-461
์ˆ˜์‹ 22-461ํ˜ธ
Classification Number
A45020.01(1)
Device Class (Risk Classification)
Class I
Classification Name
Reusable medical forceps
์žฌ์‚ฌ์šฉ๊ฐ€๋Šฅ์˜๋ฃŒ์šฉ๊ฒธ์ž
Official English Name
Forceps, reusable
Company Information
Entity Name (Company)
Sungwoo Medical Co., Ltd.
(์ฃผ)์„ฑ์šฐ๋ฉ”๋””์นผ
Entity Address
์„œ์šธํŠน๋ณ„์‹œ ์˜๋“ฑํฌ๊ตฌ ๊ตญ์ œ๊ธˆ์œต๋กœ8๊ธธ 27-9 1010ํ˜ธ(์—ฌ์˜๋„๋™,๋™๋ถ๋นŒ๋”ฉ)
Manufacturer
EYEGEN MEDICAL LLP
Category
Import business
์ˆ˜์ž…์—…
Business License Number
์ œ 110 ํ˜ธ
Important Dates & Status
Item Approval Date
Mar 18, 2022
Business Permit Date
Oct 20, 2004
Expiration Period
2022-03-18 ~ 2027-03-17
For Export
์•„๋‹ˆ์˜ค
Model Information
Model Name
EBP07025-53A and one other case
EBP07025-53A์™ธ 1๊ฑด
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing