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"Bidi" eye scalpel (sterilized) - Taiwan Registration 716f1d3d20b657e10f336b11a7ad8171

Access comprehensive regulatory information for "Bidi" eye scalpel (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 716f1d3d20b657e10f336b11a7ad8171 and manufactured by BD OPHTHALMIC SYSTEMS. The authorized representative in Taiwan is BOULDER ENTERPRISE 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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716f1d3d20b657e10f336b11a7ad8171
Registration Details
Taiwan FDA Registration: 716f1d3d20b657e10f336b11a7ad8171
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Device Details

"Bidi" eye scalpel (sterilized)
TW: "ๅฟ…ๅธ"็œผ็ง‘ๆ‰‹่ก“ๅˆ€(ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

716f1d3d20b657e10f336b11a7ad8171

DHA04400400000

Company Information

United Kingdom

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".

M Ophthalmology

M.4350 ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

Input;; QMS/QSD

Dates and Status

Apr 17, 2006

Apr 17, 2011

Nov 09, 2012

Cancellation Information

Logged out

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