Taiwan FDA registration 29ad1982700aaf803998a7edf4b787f5
"Tongdalup" inspection glasses and their accessories (unsterilized)
TW: “通達樂”檢查鏡及其附件 (未滅菌)
Taiwan·Risk Class 1·TONTARRA MEDIZINTECHNIK GMBH·Registered Feb 20, 2013 – Feb 20, 2018CancelledRegistration details
- Analysis ID
- 29ad1982700aaf803998a7edf4b787f5
- Customs Code
- DHA04401272300
Company information
- Manufacturer
- TONTARRA MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- PLOVER MEDICAL INSTRUMENTS, INC.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Examination Scopes and Their Accessories (I.1800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.1800 Inspection Scopes and Annexes
- Import Information
- import
Dates and status
- Registration Date
- Feb 20, 2013
- Expiry Date
- Feb 20, 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 "Tongdalup" inspection glasses and their accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 29ad1982700aaf803998a7edf4b787f5 and manufactured by TONTARRA MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is PLOVER MEDICAL INSTRUMENTS, INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices