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“Bausch + Lomb”Otolaryngology Manual Surgical Instruments (Non-Sterile) - Taiwan Registration 3b71535defd39686ae0aa5cd8d304fbd

Access comprehensive regulatory information for “Bausch + Lomb”Otolaryngology Manual Surgical Instruments (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 3b71535defd39686ae0aa5cd8d304fbd 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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Registration Details
Taiwan FDA Registration: 3b71535defd39686ae0aa5cd8d304fbd
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Device Details

“Bausch + Lomb”Otolaryngology Manual Surgical Instruments (Non-Sterile)
TW: “博士倫”耳鼻喉手動式外科器械 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

3b71535defd39686ae0aa5cd8d304fbd

Ministry of Health Medical Device Import No. 013376

DHA09401337600

Company Information

United States

Product Details

G ENT device

G4420 OTOLARYNGARY Manual Surgical Instrument

Imported from abroad

Dates and Status

Sep 04, 2013

Sep 04, 2018

May 19, 2022

Cancellation Information

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