Taiwan FDA registration 2e1a7774264f87f6ced765f861dbd3e7
"Kaile" retinal scope (unsterilized)
TW: "凱樂"視網膜鏡（未滅菌）
Taiwan·Risk Class 1·KEELER LTD.·Registered Apr 10, 2006 – Apr 10, 2026ExpiredRegistration details
- Analysis ID
- 2e1a7774264f87f6ced765f861dbd3e7
- Customs Code
- DHA04400351301
Company information
- Manufacturer
- KEELER LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- TAIWAN OPTICAL CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment "Retinal Scope (M.1780) First Grade Identification Range.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1780 Retinal Lens
- Import Information
- import
Dates and status
- Registration Date
- Apr 10, 2006
- Expiry Date
- Apr 10, 2026
About this record
Access comprehensive regulatory information for "Kaile" retinal scope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2e1a7774264f87f6ced765f861dbd3e7 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