Taiwan FDA registration 2b88fc237eda5bc9bf21b38d92863964
"I.C.P." Keratoscope (Non-Sterile)
TW: "艾希匹" 角膜鏡 (未滅菌)
Taiwan·Risk Class 1·MD·SBM SISTEMI·Registered Mar 29, 2017 – Mar 29, 2022CancelledRegistration details
- Analysis ID
- 2b88fc237eda5bc9bf21b38d92863964
- License Form
- Ministry of Health Medical Device Import No. 017655
- Customs Code
- DHA09401765501
Company information
- Manufacturer
- SBM SISTEMI
- Manufacturer Country
- Italy
- Authorized Representative
- TAIWAN OPTICAL CO., LTD.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1350 Keatoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 29, 2017
- Expiry Date
- Mar 29, 2022
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "I.C.P." Keratoscope (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2b88fc237eda5bc9bf21b38d92863964 and manufactured by SBM SISTEMI. The authorized representative in Taiwan is TAIWAN OPTICAL CO., LTD..
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