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Stryker inflatable tourniquet (non-sterile) - Taiwan Registration 98c6e5fe9731f209df7a296f860f756d

Access comprehensive regulatory information for Stryker inflatable tourniquet (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 98c6e5fe9731f209df7a296f860f756d and manufactured by STRYKER INSTRUMENTS;; IMED Medical Mexicana, S. de R.L. de C. V.. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.

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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98c6e5fe9731f209df7a296f860f756d
Registration Details
Taiwan FDA Registration: 98c6e5fe9731f209df7a296f860f756d
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Device Details

Stryker inflatable tourniquet (non-sterile)
TW: "ๅฒ่ณฝๅ…‹" ๅ……ๆฐฃๅผๆญข่ก€ๅธถ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

98c6e5fe9731f209df7a296f860f756d

DHA09402364303

Company Information

Product Details

It is limited to the first level of identification scope of the "Inflatable Tourniquet (I.5910)" of the classification and grading management measures for medical equipment.

I General, Plastic Surgery and Dermatology

I.5910 ๅ……ๆฐฃๅผๆญข่ก€ๅธถ

ๅง”่จ—่ฃฝ้€ ;; ่ผธๅ…ฅ;; QMS/QSD

Dates and Status

Oct 25, 2024

Oct 25, 2029