Taiwan FDA registration 626cd7d39f823595b11048231b10c7b4
“Keeler” Indirect Ophthalmoscope and Accessories
TW: “奇勒” 間接眼底鏡及其附件
Taiwan·Risk Class 2·MD·Keeler Limited·Registered Oct 31, 2013 – Oct 31, 2028ActiveRegistration details
- Analysis ID
- 626cd7d39f823595b11048231b10c7b4
- License Form
- Ministry of Health Medical Device Import No. 025572
- Customs Code
- DHA05602557209
Company information
- Manufacturer
- Keeler Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EVERLIGHT INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1570 fundus mirror
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 31, 2013
- Expiry Date
- Oct 31, 2028
About this record
Access comprehensive regulatory information for “Keeler” Indirect Ophthalmoscope and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 626cd7d39f823595b11048231b10c7b4 and manufactured by Keeler Limited. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT 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