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"Snei-fai" Interrio 4K camera system - Taiwan Registration bd97be1d664c412a4fc2a02081fc3008

Access comprehensive regulatory information for "Snei-fai" Interrio 4K camera system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bd97be1d664c412a4fc2a02081fc3008 and manufactured by SMITH & NEPHEW INC., ENDOSCOPY DIVISION;; SMITH & NEPHEW INC. ENDOSCOPY DIVISION. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).

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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bd97be1d664c412a4fc2a02081fc3008
Registration Details
Taiwan FDA Registration: bd97be1d664c412a4fc2a02081fc3008
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Device Details

"Snei-fai" Interrio 4K camera system
TW: โ€œๅฒ่€่ผโ€่‹ฑ็‰น้‡Œๆญ4Kๆ”ๅฝฑๆฉŸ็ณป็ตฑ
Risk Class 2

Registration Details

bd97be1d664c412a4fc2a02081fc3008

DHA05603715002

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Apr 23, 2024

Apr 23, 2029