Taiwan FDA registration 5050bb9f3455c1d28c4e62cc366c067a
"Heini" indirect fundus lens and accessories
TW: “海尼”間接眼底鏡及附件
Taiwan·Risk Class 2·HEINE OPTOTECHNIK GMBH & CO. KG·Registered Mar 08, 2007 – Mar 08, 2012CancelledRegistration details
- Analysis ID
- 5050bb9f3455c1d28c4e62cc366c067a
- Customs Code
- DHA00601777702
Company information
- Manufacturer
- HEINE OPTOTECHNIK GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- Poussen Industrial Limited
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1570 Fundus Mirrors
- Import Information
- import
Dates and status
- Registration Date
- Mar 08, 2007
- Expiry Date
- Mar 08, 2012
- Cancellation Date
- May 05, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Heini" indirect fundus lens and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5050bb9f3455c1d28c4e62cc366c067a and manufactured by HEINE OPTOTECHNIK GMBH & CO. KG. The authorized representative in Taiwan is Poussen Industrial Limited.
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