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"Bausch & Len" high-speed vitrectomy surgical kit - Taiwan Registration e57f52f97db7ea5d2a2456469d9ec778

Access comprehensive regulatory information for "Bausch & Len" high-speed vitrectomy surgical kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e57f52f97db7ea5d2a2456469d9ec778 and manufactured by BAUSCH & LOMB INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.

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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e57f52f97db7ea5d2a2456469d9ec778
Registration Details
Taiwan FDA Registration: e57f52f97db7ea5d2a2456469d9ec778
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Device Details

"Bausch & Len" high-speed vitrectomy surgical kit
TW: โ€œๅšๅฃซๅ€ซโ€้ซ˜้€Ÿ็Žป็’ƒ้ซ”ๅˆ‡้™คๆ‰‹่ก“ๅŒ…
Risk Class 2
Cancelled

Registration Details

e57f52f97db7ea5d2a2456469d9ec778

DHA00602092205

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmology

M.4150 Vitreous Suction and Cutting Apparatus

import

Dates and Status

Apr 21, 2010

Apr 21, 2020

May 19, 2022

Cancellation Information

Logged out

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