Taiwan FDA registration 2a73608864687d37671d78549fa6fe05
Headlamp for the "Pireody" procedure (unsterilized)
TW: "倍銳歐帝"手術用頭燈(未滅菌)
Taiwan·Risk Class 1·PERIOPTIX INC.·Registered Nov 28, 2011 – Nov 28, 2016CancelledRegistration details
- Analysis ID
- 2a73608864687d37671d78549fa6fe05
- Customs Code
- DHA04401111304
Company information
- Manufacturer
- PERIOPTIX INC.
- Manufacturer Country
- United States
- Authorized Representative
- INTERLINK MEDICAL ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Surgical Headlamps (M.4335)".
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4335 Headlamps for surgery
- Import Information
- import
Dates and status
- Registration Date
- Nov 28, 2011
- Expiry Date
- Nov 28, 2016
- Cancellation Date
- Jun 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Headlamp for the "Pireody" procedure (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2a73608864687d37671d78549fa6fe05 and manufactured by PERIOPTIX INC.. The authorized representative in Taiwan is INTERLINK MEDICAL ENTERPRISE CO., LTD..
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