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"DGH" Keratoscope (Non-Sterile) - Taiwan Registration 2e9255a3eb34f53bfaacec3b50ddc3f5

Access comprehensive regulatory information for "DGH" 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 2e9255a3eb34f53bfaacec3b50ddc3f5 and manufactured by DGH Technology Inc.. The authorized representative in Taiwan is Kangcheng Biomedical Technology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DGH Technology Inc., and 1 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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2e9255a3eb34f53bfaacec3b50ddc3f5
Registration Details
Taiwan FDA Registration: 2e9255a3eb34f53bfaacec3b50ddc3f5
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Device Details

"DGH" Keratoscope (Non-Sterile)
TW: "่ฟชๅฑ…ๆ›ฒ" ่ง’่†œ้ก (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

2e9255a3eb34f53bfaacec3b50ddc3f5

Ministry of Health Medical Device Import Registration No. 017752

DHA08401775200

Company Information

United States

Product Details

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2022

Cancellation Information

Logged out

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