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“SHI SEI”Saliva Ejector (Non-Sterile) - Taiwan Registration 737c043e92c212a07f13d907115ca683

Access comprehensive regulatory information for “SHI SEI”Saliva Ejector (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 737c043e92c212a07f13d907115ca683 and manufactured by WORLD WORK S.R.L.. The authorized representative in Taiwan is SHI SEI INTERNATIONAL 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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737c043e92c212a07f13d907115ca683
Registration Details
Taiwan FDA Registration: 737c043e92c212a07f13d907115ca683
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Device Details

“SHI SEI”Saliva Ejector (Non-Sterile)
TW: “資生”吸唾管 (未滅菌)
Risk Class 1
MD

Registration Details

737c043e92c212a07f13d907115ca683

Ministry of Health Medical Device Import No. 013568

DHA09401356809

Company Information

Italy

Product Details

Limited to the first level identification range of dental surgical devices and their accessories (F.6640) under the Measures for the Administration of Medical Devices.

F Dental devices

F6640 Dental Surgical Devices and Their Accessories

Imported from abroad

Dates and Status

Nov 07, 2013

Nov 07, 2023