Taiwan FDA registration ee42a5a45a3f2a0d08c2924abe09f995
"Heini" direct fundus lens and accessories
TW: “海尼”直接眼底鏡及附件
Taiwan·Risk Class 2·HEINE OPTOTECHNIK GMBH & CO. KG·Registered Jun 12, 2007 – Jun 12, 2012CancelledRegistration details
- Analysis ID
- ee42a5a45a3f2a0d08c2924abe09f995
- Customs Code
- DHA00601811803
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
- Jun 12, 2007
- Expiry Date
- Jun 12, 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" direct 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 ee42a5a45a3f2a0d08c2924abe09f995 and manufactured by HEINE OPTOTECHNIK GMBH & CO. KG. The authorized representative in Taiwan is Poussen Industrial Limited.
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