Taiwan FDA registration bf19ed887a72c364d74daca0add472c8
"Karst" electronic duodenoscopy and its accessories
TW: “卡爾斯特”電子式十二指腸鏡及其附件
Taiwan·Risk Class 2·KARL STROZ GMBH & CO., KG·Registered Mar 12, 2008 – Mar 12, 2018CancelledRegistration details
- Analysis ID
- bf19ed887a72c364d74daca0add472c8
- Customs Code
- DHA00601864003
Company information
- Manufacturer
- KARL STROZ GMBH & CO., KG
- Manufacturer Country
- Germany
- Authorized Representative
- KARL STORZ ENDOSCOPY TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Mar 12, 2008
- Expiry Date
- Mar 12, 2018
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Karst" electronic duodenoscopy and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bf19ed887a72c364d74daca0add472c8 and manufactured by KARL STROZ GMBH & CO., KG. The authorized representative in Taiwan is KARL STORZ ENDOSCOPY TAIWAN LTD..
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