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"Guise" ENT manual surgical instruments (unsterilized)  - Taiwan Registration 32633d2071fc56cde75dda2f42fd1e2c

Access comprehensive regulatory information for "Guise" ENT manual surgical instruments (unsterilized)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 32633d2071fc56cde75dda2f42fd1e2c and manufactured by GYRUS ENT LLC. The authorized representative in Taiwan is MEDFRONT MEDICAL TECHNOLOGY CORPORATION.

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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32633d2071fc56cde75dda2f42fd1e2c
Registration Details
Taiwan FDA Registration: 32633d2071fc56cde75dda2f42fd1e2c
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Device Details

"Guise" ENT manual surgical instruments (unsterilized) 
TW: "吉斯"耳鼻喉手動式外科器械(未滅菌) 
Risk Class 1
Cancelled

Registration Details

32633d2071fc56cde75dda2f42fd1e2c

DHA04400690300

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".

G ENT Science

G.4420 Otolaryngology manual surgical instruments

import

Dates and Status

Jul 11, 2008

Jul 11, 2013

Jun 16, 2015

Cancellation Information

Logged out

許可證已逾有效期