Taiwan FDA registration 1a6e10ff298ef64f28fdb993a2d5b5b0
"DORNIER" laser with light pipe
TW: “多尼爾”雷射用光導管
Taiwan·Risk Class 2·DORNIER MEDTECH GMBH; Dornier MedTech Laser GmbH·Registered Mar 29, 2011 – Mar 29, 2021CancelledRegistration details
- Analysis ID
- 1a6e10ff298ef64f28fdb993a2d5b5b0
- Customs Code
- DHA00602225209
Company information
- Manufacturer
- DORNIER MEDTECH GMBH; Dornier MedTech Laser GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- VICTORY EIGHT ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- import
Dates and status
- Registration Date
- Mar 29, 2011
- Expiry Date
- Mar 29, 2021
- Cancellation Date
- Jun 15, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "DORNIER" laser with light pipe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1a6e10ff298ef64f28fdb993a2d5b5b0 and manufactured by DORNIER MEDTECH GMBH; Dornier MedTech Laser GmbH. The authorized representative in Taiwan is VICTORY EIGHT ENTERPRISE CO., LTD..
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