Taiwan FDA registration 7585e7ac7ab3ddd318301a9851535afc

"KK" Battery Powered Capillaroscopy Transilluminator (Non-Sterile)

TW: "基楷" 電池式微血管透照器 (未滅菌)

Taiwan·Risk Class 1·MD·KK TECHNOLOGY LTD.·Registered Nov 08, 2013 – Nov 08, 2018Cancelled

Registration details

Analysis ID: 7585e7ac7ab3ddd318301a9851535afc
License Form: Ministry of Health Medical Device Import No. 013572
Customs Code: DHA09401357200

Company information

Manufacturer: KK TECHNOLOGY LTD.
Manufacturer Country: United Kingdom
Authorized Representative: MICROSTAR INSTRUMENTS CO., LTD.

Product details

Product Type (Level 1): M Ophthalmic devices
Product Type (Level 2): M1945 transillumination
Import Information: Imported from abroad

Dates and status

Registration Date: Nov 08, 2013
Expiry Date: Nov 08, 2018
Cancellation Date: Aug 05, 2022

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "KK" Battery Powered Capillaroscopy Transilluminator (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7585e7ac7ab3ddd318301a9851535afc and manufactured by KK TECHNOLOGY LTD.. The authorized representative in Taiwan is MICROSTAR INSTRUMENTS CO., LTD..

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