Taiwan FDA registration 98a7230c5cae19e6f757e6a448f11547

Manual Ophthalmic Surgery Instrument (Sterile)

TW: "必唯愛" 手動式眼科手術器械 (滅菌)
Taiwan flagTaiwan·Risk Class 1·BEAVER-VISITEC INTERNATIONAL, INC.·Registered Sep 16, 2011 – Sep 16, 2021Cancelled
Registration details
Analysis ID
98a7230c5cae19e6f757e6a448f11547
Customs Code
DHA04401084208
Company information
Manufacturer Country
United States
Authorized Representative
BOULDER ENTERPRISE CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.4350 手動式眼科手術器械
Import Information
import
Dates and status
Registration Date
Sep 16, 2011
Expiry Date
Sep 16, 2021
Cancellation Date
Sep 08, 2023
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for Manual Ophthalmic Surgery Instrument (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 98a7230c5cae19e6f757e6a448f11547 and manufactured by BEAVER-VISITEC INTERNATIONAL, INC.. The authorized representative in Taiwan is BOULDER ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including CARL ZEISS MEDITEC AG;; COASTLINE DE MEXICO, S.A. DE C.V., BAUSCH & LOMB INC.;; SURGICAL SPECIALTIES MEXICO, S. DE R.L. DE C.V., and 5 recent registrations in the same category. 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.

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