Taiwan FDA registration a489fb69e115569c1148870da093c15c
"Heini" rectal diagnostic scope and its accessories
TW: "海尼"直腸診斷鏡及其附件
Taiwan·Risk Class 2·HEINE OPTOTECHNIK GMBH & CO. LTD.·Registered Nov 02, 2005 – Nov 02, 2015CancelledRegistration details
- Analysis ID
- a489fb69e115569c1148870da093c15c
- Customs Code
- DHA00601290904
Company information
- Manufacturer
- HEINE OPTOTECHNIK GMBH & CO. LTD.
- Manufacturer Country
- Germany
- Authorized Representative
- SANSOME TRADING CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- Nov 02, 2005
- Expiry Date
- Nov 02, 2015
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Heini" rectal diagnostic scope 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 a489fb69e115569c1148870da093c15c and manufactured by HEINE OPTOTECHNIK GMBH & CO. LTD.. The authorized representative in Taiwan is SANSOME TRADING CO., LTD..
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