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Reusable manual medical knife

์žฌ์‚ฌ์šฉ๊ฐ€๋Šฅ์ˆ˜๋™์‹์˜๋ฃŒ์šฉ์นผ

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. 22-2198. Approved on Dec 23, 2022. Registered by DSHITECH Co., Ltd..

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MFDS Official Data
Class I
Basic Information
Item Serial Number
2022006639
License Number
Reception No. 22-2198
์ˆ˜์‹ 22-2198ํ˜ธ
Classification Number
A41010.01(1)
Device Class (Risk Classification)
Class I
Classification Name
Reusable manual medical knife
์žฌ์‚ฌ์šฉ๊ฐ€๋Šฅ์ˆ˜๋™์‹์˜๋ฃŒ์šฉ์นผ
Official English Name
Knife, manually-operated, reusable
Company Information
Entity Name (Company)
DSHITECH Co., Ltd.
(์ฃผ)๋””์—์Šคํ•˜์ดํ…
Entity Address
๊ฒฝ๊ธฐ๋„ ํ•˜๋‚จ์‹œ ์„œํ•˜๋‚จ๋กœ43๋ฒˆ๊ธธ 166 2์ธต (๊ฐ๋ถ๋™)
Manufacturer
FUJITA Medical Instruments Co., Ltd.
Category
Import business
์ˆ˜์ž…์—…
Business License Number
์ œ 73 ํ˜ธ
Important Dates & Status
Item Approval Date
Dec 23, 2022
Business Permit Date
Sep 21, 2004
Expiration Period
2022-12-23 ~ 2027-12-22
For Export
์•„๋‹ˆ์˜ค
Model Information
Model Name
8013-60 and 17 other cases
8013-60์™ธ 17๊ฑด
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