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In vitro medical electrodes

์ฒด์™ธํ˜•์˜๋ฃŒ์šฉ์ „๊ทน

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. 22-528. Approved on Mar 28, 2022. Registered by Philips Korea Co., Ltd..

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MFDS Official Data
Class I
Basic Information
Item Serial Number
2022001586
License Number
Reception No. 22-528
์ˆ˜์‹ 22-528ํ˜ธ
Classification Number
A58060.01(1)
Device Class (Risk Classification)
Class I
Classification Name
In vitro medical electrodes
์ฒด์™ธํ˜•์˜๋ฃŒ์šฉ์ „๊ทน
Official English Name
Electrode, external
Company Information
Entity Name (Company)
Philips Korea Co., Ltd.
(์ฃผ)ํ•„๋ฆฝ์Šค์ฝ”๋ฆฌ์•„
Entity Address
์„œ์šธํŠน๋ณ„์‹œ ์ค‘๊ตฌ ์†Œ์›”๋กœ2๊ธธ 30 (๋‚จ๋Œ€๋ฌธ๋กœ5๊ฐ€)
Manufacturer
Covidien
Category
Import business
์ˆ˜์ž…์—…
Business License Number
์ œ 1246 ํ˜ธ
Important Dates & Status
Item Approval Date
Mar 28, 2022
Business Permit Date
May 29, 2006
Expiration Period
2020-10-08 ~ 2025-08-31
For Export
์•„๋‹ˆ์˜ค
Model Information
Model Name
13952A and 1 other case
13952A์™ธ 1๊ฑด
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DJ Fang

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