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“BERNELL”Stereoscope (Non-Sterile) - Taiwan Registration a139bec8dbbb5ef3219a7c0ac1e0998b

Access comprehensive regulatory information for “BERNELL”Stereoscope (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 a139bec8dbbb5ef3219a7c0ac1e0998b and manufactured by BERNELL CORPORATION. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BERNELL CORPORATION, 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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a139bec8dbbb5ef3219a7c0ac1e0998b
Registration Details
Taiwan FDA Registration: a139bec8dbbb5ef3219a7c0ac1e0998b
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Device Details

“BERNELL”Stereoscope (Non-Sterile)
TW: “博尼”立體鏡 (未滅菌)
Risk Class 1
MD

Registration Details

a139bec8dbbb5ef3219a7c0ac1e0998b

Ministry of Health Medical Device Import Registration No. 022458

DHA08402245807

Company Information

United States

Product Details

Limited to the first-level identification range of the medical equipment management measures "stereoscope (M.1870)".

M Ophthalmic devices

M1870 stereoscope

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026

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