South Korea MFDS registration Reception No. 22-840

Manual vasodilator

KO: 수동식혈관확장기
South Korea flagSouth Korea·Class I·PrimeMed Inc.·Approved May 12, 2022
Basic information
Item Serial Number
2022002463
License Number
Reception No. 22-840
수신22-840호
Classification Number
A59010.01(1)
Device Class (Risk Classification)
Class I
Classification Name
Manual vasodilator
수동식혈관확장기
Official English Name
Dilator, vascular, manually-operated
Company information
Entity Name (Company)
PrimeMed Inc.
(주)프라임메드
Entity Address
경기도 성남시 수정구 성남대로 1244 , 107 (태평동, 인티움)
Manufacturer
Novo Surgical
Category
Import business
수입업
Business License Number
제 1570 호
Important dates & status
Item Approval Date
May 12, 2022
Business Permit Date
Jan 18, 2008
Expiration Period
2022-05-12 ~ 2027-05-11
For Export
아니오
Model information
Model Name
5570-02 and 42 other cases
5570-02외 42건
About this record

This Class I medical device is registered with South Korea's Ministry of Food and Drug Safety (MFDS / 식품의약품안전처) under license number Reception No. 22-840. Approved on May 12, 2022. Registered by PrimeMed Inc..

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