Taiwan FDA registration 8ba9bd3098f60e162a5f31c7997924cc
"Beaver-Visitec" Manual Ophthalmic Surgical Instrument (non-sterile)
TW: "畢威艾"手動式眼科手術器械(未滅菌)
Registration details
- Analysis ID
- 8ba9bd3098f60e162a5f31c7997924cc
- License Form
- Ministry of Health Medical Device Import No. 015963
- Customs Code
- DHA09401596302
Company information
- Manufacturer
- BEAVER-VISITEC INTERNATIONAL, INC.
- Manufacturer Country
- United States
- Authorized Representative
- CLINICO INC.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M4350 Manual Ophthalmic Surgery Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 11, 2015
- Expiry Date
- Dec 11, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Beaver-Visitec" Manual Ophthalmic Surgical Instrument (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 8ba9bd3098f60e162a5f31c7997924cc and manufactured by BEAVER-VISITEC INTERNATIONAL, INC.. The authorized representative in Taiwan is CLINICO INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices