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“STRENGTHEN” INFUSION STAND (Non-Sterile) - Taiwan Registration ccfc79e55d1729b1f4d4e2c5e56afc22

Access comprehensive regulatory information for “STRENGTHEN” INFUSION STAND (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 ccfc79e55d1729b1f4d4e2c5e56afc22 and manufactured by LINET SPOL. S R. O.. The authorized representative in Taiwan is Johnson & Johnson Medical Instruments 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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ccfc79e55d1729b1f4d4e2c5e56afc22
Registration Details
Taiwan FDA Registration: ccfc79e55d1729b1f4d4e2c5e56afc22
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Device Details

“STRENGTHEN” INFUSION STAND (Non-Sterile)
TW: “強生” 注射架 (未滅菌)
Risk Class 1
MD

Registration Details

ccfc79e55d1729b1f4d4e2c5e56afc22

Ministry of Health Medical Device Import No. 021488

DHA09402148807

Company Information

Czechia

Product Details

Limited to the first level identification range of the "Injection Rack (J.6990)" of the Measures for the Administration of Medical Equipment.

J General hospital and personal use equipment

J6990 Injection rack

Imported from abroad

Dates and Status

Apr 27, 2020

Apr 27, 2025