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"WELCH ALLYN" Keratoscope (Non-Sterile) - Taiwan Registration 846ee77049c800355821b10dcd190580

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..

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.

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846ee77049c800355821b10dcd190580
Registration Details
Taiwan FDA Registration: 846ee77049c800355821b10dcd190580
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Device Details

"WELCH ALLYN" Keratoscope (Non-Sterile)
TW: "ๅจๆ ฉ้ˆ" ่ง’่†œ้ก (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

846ee77049c800355821b10dcd190580

Ministry of Health Medical Device Import No. 019265

DHA09401926508

Company Information

United States

Product Details

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Jul 04, 2018

Jul 04, 2023

Cancellation Information

Logged out

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