Taiwan FDA registration 51317b8e292a8677ff06b0a8fd52b89f
“Keeler” Slit Lamp and accessories
TW: “奇勒”裂隙燈及其附件
Taiwan·Risk Class 2·MD·KEELER LTD.·Registered Mar 28, 2019 – Mar 28, 2024ExpiredRegistration details
- Analysis ID
- 51317b8e292a8677ff06b0a8fd52b89f
- License Form
- Ministry of Health Medical Device Import No. 032319
- Customs Code
- DHA05603231901
Company information
- Manufacturer
- KEELER LTD.
- 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
- Mar 28, 2019
- Expiry Date
- Mar 28, 2024
About this record
Access comprehensive regulatory information for “Keeler” 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 51317b8e292a8677ff06b0a8fd52b89f and manufactured by KEELER LTD.. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT CO., LTD..
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