Taiwan FDA registration 5eb6e267081044d3bdea88cc6399dad4
“Keeler” Portable Slit Lamp and accessories
TW: “奇勒”手持式裂隙燈及其附件
Taiwan·Risk Class 2·MD·Keeler Limited·Registered May 25, 2016 – May 25, 2026ExpiredRegistration details
- Analysis ID
- 5eb6e267081044d3bdea88cc6399dad4
- License Form
- Ministry of Health Medical Device Import No. 028542
- Customs Code
- DHA05602854202
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)
- M1850 AC power type fine gap lamp
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 25, 2016
- Expiry Date
- May 25, 2026
About this record
Access comprehensive regulatory information for “Keeler” Portable Slit Lamp 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 5eb6e267081044d3bdea88cc6399dad4 and manufactured by Keeler Limited. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT CO., LTD..
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