Taiwan FDA registration 8b718fccf74705557f07b462dbd5bc5a
“Keeler” Cryophthalmic unit and accessories
TW: “奇勒”眼科冷凍儀及其附件
Taiwan·Risk Class 2·MD·Keeler Limited·Registered Jul 31, 2013 – Jul 31, 2028ActiveRegistration details
- Analysis ID
- 8b718fccf74705557f07b462dbd5bc5a
- License Form
- Ministry of Health Medical Device Import No. 025312
- Customs Code
- DHA05602531209
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)
- M4170 Eye Cryometer
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 31, 2013
- Expiry Date
- Jul 31, 2028
About this record
Access comprehensive regulatory information for “Keeler” Cryophthalmic unit 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 8b718fccf74705557f07b462dbd5bc5a and manufactured by Keeler Limited. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT CO., LTD..
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