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“Laerdal” Suction Unit - Taiwan Registration 84b258d7af67e06d5d96ad0a79bc8bd5

Access comprehensive regulatory information for “Laerdal” Suction Unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 84b258d7af67e06d5d96ad0a79bc8bd5 and manufactured by LAERDAL MEDICAL AS. The authorized representative in Taiwan is TAIWAN MEDICAL SERVICES 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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84b258d7af67e06d5d96ad0a79bc8bd5
Registration Details
Taiwan FDA Registration: 84b258d7af67e06d5d96ad0a79bc8bd5
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Device Details

“Laerdal” Suction Unit
TW: “洛德”動力式抽吸幫浦
Risk Class 2
MD

Registration Details

84b258d7af67e06d5d96ad0a79bc8bd5

Ministry of Health Medical Device Import No. 034811

DHA05603481102

Company Information

Norway

Product Details

Details are as detailed as approved Chinese instructions

I General and plastic surgical devices

I4780 powered suction pump

Imported from abroad

Dates and Status

Aug 07, 2021

Aug 07, 2026