Taiwan FDA registration 846ee77049c800355821b10dcd190580
"WELCH ALLYN" Keratoscope (Non-Sterile)
TW: "威栩靈" 角膜鏡 (未滅菌)
Taiwan·Risk Class 1·MD·WELCH ALLYN INC.·Registered Jul 04, 2018 – Jul 04, 2023CancelledRegistration details
- Analysis ID
- 846ee77049c800355821b10dcd190580
- License Form
- Ministry of Health Medical Device Import No. 019265
- Customs Code
- DHA09401926508
Company information
- Manufacturer
- WELCH ALLYN INC.
- Manufacturer Country
- United States
- Authorized Representative
- BIOMEGA INSTRUMENT 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
- Jul 04, 2018
- Expiry Date
- Jul 04, 2023
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "WELCH ALLYN" 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 846ee77049c800355821b10dcd190580 and manufactured by WELCH ALLYN INC.. The authorized representative in Taiwan is BIOMEGA INSTRUMENT CO., LTD..
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