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Endovascular sphygmomanometer

ํ˜ˆ๊ด€๋‚ดํ˜ˆ์••๊ณ„

This Class II medical device is registered with South Korea's Ministry of Food and Drug Safety (MFDS / ์‹ํ’ˆ์˜์•ฝํ’ˆ์•ˆ์ „์ฒ˜) under license number Suin No. 22-4224. Approved on Apr 27, 2022. Registered by Philips Korea Co., Ltd..

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MFDS Official Data
Class II
Basic Information
Item Serial Number
2022002174
License Number
Suin No. 22-4224
์ˆ˜์ธ22-4224ํ˜ธ
Classification Number
A23020.01(2)
Device Class (Risk Classification)
Class II
Classification Name
Endovascular sphygmomanometer
ํ˜ˆ๊ด€๋‚ดํ˜ˆ์••๊ณ„
Official English Name
Manometer, blood-pressure, venous
Company Information
Entity Name (Company)
Philips Korea Co., Ltd.
(์ฃผ)ํ•„๋ฆฝ์Šค์ฝ”๋ฆฌ์•„
Entity Address
์„œ์šธํŠน๋ณ„์‹œ ์ค‘๊ตฌ ์†Œ์›”๋กœ2๊ธธ 30 (๋‚จ๋Œ€๋ฌธ๋กœ5๊ฐ€)
Manufacturer
Philips de Costa Rica S.R.L
Category
Import business
์ˆ˜์ž…์—…
Business License Number
์ œ 1246 ํ˜ธ
Important Dates & Status
Item Approval Date
Apr 27, 2022
Business Permit Date
May 29, 2006
Expiration Period
2022-04-27 ~ 2027-04-26
For Export
์•„๋‹ˆ์˜ค
Model Information
Model Name
89185 and 1 other cases
89185์™ธ 1๊ฑด
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