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Reusable medical ligators

์žฌ์‚ฌ์šฉ๊ฐ€๋Šฅ์˜๋ฃŒ์šฉ๊ฒฐ์ฐฐ๊ธฐ

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. 21-1629. Approved on Aug 31, 2021. Registered by Teleflex Korea.

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MFDS Official Data
Class I
Basic Information
Item Serial Number
2021004834
License Number
Reception No. 21-1629
์ˆ˜์‹ 21-1629ํ˜ธ
Classification Number
A38020.01(1)
Device Class (Risk Classification)
Class I
Classification Name
Reusable medical ligators
์žฌ์‚ฌ์šฉ๊ฐ€๋Šฅ์˜๋ฃŒ์šฉ๊ฒฐ์ฐฐ๊ธฐ
Official English Name
Ligature implanting instrumentation, endoscopic
Company Information
Entity Name (Company)
Teleflex Korea
ํ…”๋ ˆํ”Œ๋ ‰์Šค์ฝ”๋ฆฌ์•„(์œ )
Entity Address
์„œ์šธํŠน๋ณ„์‹œ ์ค‘๊ตฌ ์น ํŒจ๋กœ 37 10์ธต (๋ด‰๋ž˜๋™1๊ฐ€)
Manufacturer
BAUER & HASELBARTH-CHIRURG GMBH
Category
Import business
์ˆ˜์ž…์—…
Business License Number
์ œ 3358 ํ˜ธ
Important Dates & Status
Item Approval Date
Aug 31, 2021
Business Permit Date
Jun 19, 2014
Expiration Period
2021-08-31 ~ 2026-08-30
For Export
์•„๋‹ˆ์˜ค
Model Information
Model Name
353206
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DJ Fang

DJ Fang

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