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“SEIRIN” ACUPUNCTURE NEEDLES - Taiwan Registration fa0d389166096b1f563a4b3ce4088a17

Access comprehensive regulatory information for “SEIRIN” ACUPUNCTURE NEEDLES in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fa0d389166096b1f563a4b3ce4088a17 and manufactured by SEIRIN Corporation. The authorized representative in Taiwan is GREAT KUEI TAI INC..

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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fa0d389166096b1f563a4b3ce4088a17
Registration Details
Taiwan FDA Registration: fa0d389166096b1f563a4b3ce4088a17
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Device Details

“SEIRIN” ACUPUNCTURE NEEDLES
TW: “清鈴”針灸針
Risk Class 2
MD

Registration Details

fa0d389166096b1f563a4b3ce4088a17

Ministry of Health Medical Device Import No. 027783

DHA05602778306

Company Information

Japan

Product Details

For details, it is Chinese approved copy of the imitation order

J General hospital and personal use equipment

J5580 Acupuncture needles

Imported from abroad

Dates and Status

Sep 15, 2015

Sep 15, 2025