Pure Global

Reusable pleural peritoneal needle

์žฌ์‚ฌ์šฉ๊ฐ€๋Šฅํ‰๋ง‰๋ณต๋ง‰์นจ

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 Seoul Reception Room 10-2690. Approved on Nov 19, 2010. Registered by Woojin Ascending Co., Ltd..

Pure Global AI provides free access to comprehensive South Korea MFDS registration data, helping global MedTech companies analyze market presence and regulatory compliance for medical devices in South Korea.

Free Database
Powered by Pure Global AI
MFDS Official Data
Class I
Basic Information
Item Serial Number
2010006490
License Number
Seoul Reception Room 10-2690
์„œ์šธ์ˆ˜์‹ 10-2690ํ˜ธ
Classification Number
A53040.08(1)
Device Class (Risk Classification)
Class I
Classification Name
Reusable pleural peritoneal needle
์žฌ์‚ฌ์šฉ๊ฐ€๋Šฅํ‰๋ง‰๋ณต๋ง‰์นจ
Official English Name
Needle, pneumoperitoneal, reusable
Company Information
Entity Name (Company)
Woojin Ascending Co., Ltd.
(์ฃผ)์šฐ์ง„์ƒํ–‰
Entity Address
์„œ์šธํŠน๋ณ„์‹œ ์†กํŒŒ๊ตฌ ๋ฐฑ์ œ๊ณ ๋ถ„๋กœ32๊ธธ 34 ๋™์€๋นŒ๋”ฉ 2์ธต (์‚ผ์ „๋™)
Manufacturer
Jarit GmbH
Category
Import business
์ˆ˜์ž…์—…
Business License Number
์ œ 984 ํ˜ธ
Important Dates & Status
Item Approval Date
Nov 19, 2010
Business Permit Date
Jun 27, 2005
Current Situation/Status
์ทจํ•˜
For Export
์•„๋‹ˆ์˜ค
Model Information
Model Name
600-480 et al. 1 case
600-480์™ธ 1๊ฑด
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing