Taiwan FDA registration c09b7fded71d96ce45a10b1f14457b9b
Kjeldahl battery-based microvascular transilluminator (unsterilized)
TW: “凱氏”電池式微血管透照器 (未滅菌)
Taiwan·Risk Class 1·KK TECHNOLOGY LTD.·Registered Feb 02, 2007 – Feb 02, 2017CancelledRegistration details
- Analysis ID
- c09b7fded71d96ce45a10b1f14457b9b
- Customs Code
- DHA04400557800
Company information
- Manufacturer
- KK TECHNOLOGY LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SHIN CHEN INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Translucent Apparatus (M.1945)".
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1945 Transilluminator
- Import Information
- import
Dates and status
- Registration Date
- Feb 02, 2007
- Expiry Date
- Feb 02, 2017
- Cancellation Date
- Nov 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Kjeldahl battery-based microvascular transilluminator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c09b7fded71d96ce45a10b1f14457b9b and manufactured by KK TECHNOLOGY LTD.. The authorized representative in Taiwan is SHIN CHEN INSTRUMENT CO., LTD..
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