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SURFLASH "TERUMO" - Taiwan Registration 9ffb8edc3042105b134b8be8703d5ce3

Access comprehensive regulatory information for SURFLASH "TERUMO" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9ffb8edc3042105b134b8be8703d5ce3 and manufactured by KOFU FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..

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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9ffb8edc3042105b134b8be8703d5ce3
Registration Details
Taiwan FDA Registration: 9ffb8edc3042105b134b8be8703d5ce3
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Device Details

SURFLASH "TERUMO"
TW: ็ด—็ˆพ็บŒ้œ่„ˆ็•™็ฝฎ้‡
Risk Class 2
MD

Registration Details

9ffb8edc3042105b134b8be8703d5ce3

Department of Health Medical Device Import No. 009217

DHA00600921704

Company Information

Product Details

1399 Other blood transfusion, infusion equipment

Imported from abroad

Dates and Status

Jun 25, 1999

Feb 09, 2029