South Korea MFDS registration Reception No. 22-1901
Reusable endoscopic cannula
KO: 재사용가능내시경캐뉼러
South Korea·Class I·Asrex Korea·Approved Nov 07, 2022Basic information
- Item Serial Number
- 2022005668
- License Number
- Reception No. 22-1901
- Classification Number
- A31010.22(1)
- Device Class (Risk Classification)
- Class I
- Classification Name
- Reusable endoscopic cannula
- Official English Name
- Endotherapy cannula, reusable
수신22-1901호
재사용가능내시경캐뉼러
Company information
- Entity Address
- 서울특별시 강남구 테헤란로 521 20층(삼성동)
- Manufacturer
- Henke Sass Wolf GmbH
- Category
- Import business
- Business License Number
- 제 4030 호
수입업
Important dates & status
- Item Approval Date
- Nov 07, 2022
- Business Permit Date
- Feb 13, 2017
- Expiration Period
- 2022-11-07 ~ 2027-11-06
- For Export
- 아니오
Model information
- Model Name
- AR-3320-02 and 1 other case
AR-3320-02외 1건
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. 22-1901. Approved on Nov 07, 2022. Registered by Asrex Korea.
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