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Bone forceps

๊ณจ๊ฒธ์ž

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. 23-3. Approved on Jan 02, 2023. Registered by DSHITECH Co., Ltd..

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MFDS Official Data
Class I
Basic Information
Item Serial Number
2023000005
License Number
Reception No. 23-3
์ˆ˜์‹ 23-3ํ˜ธ
Classification Number
A45020.05(1)
Device Class (Risk Classification)
Class I
Classification Name
Bone forceps
๊ณจ๊ฒธ์ž
Official English Name
Forceps, bone
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 Instrumetns Co., Ltd.
Category
Import business
์ˆ˜์ž…์—…
Business License Number
์ œ 73 ํ˜ธ
Important Dates & Status
Item Approval Date
Jan 02, 2023
Business Permit Date
Sep 21, 2004
Expiration Period
2023-01-02 ~ 2028-01-01
For Export
์•„๋‹ˆ์˜ค
Model Information
Model Name
8211-10 and 10 other cases
8211-10์™ธ 10๊ฑด
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