Taiwan FDA registration 9f5c44fbcd3596093592f7297a1fde30
"Kaile" surgical magnifying glass and accessories (unsterilized)
TW: "凱樂" 手術放大鏡及附件(未滅菌)
Taiwan·Risk Class 1·KEELER LTD.·Registered Mar 29, 2006 – Mar 29, 2026CancelledRegistration details
- Analysis ID
- 9f5c44fbcd3596093592f7297a1fde30
- Customs Code
- DHA04400328001
Company information
- Manufacturer
- KEELER LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- TAIWAN OPTICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices (Ophthalmic Surgical Glasses [M.4770]).
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4770 Ophthalmic surgical lenses (magnifying lenses)
- Import Information
- import
Dates and status
- Registration Date
- Mar 29, 2006
- Expiry Date
- Mar 29, 2026
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Kaile" surgical magnifying glass and 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 9f5c44fbcd3596093592f7297a1fde30 and manufactured by KEELER LTD.. The authorized representative in Taiwan is TAIWAN OPTICAL CO., LTD..
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