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"Stryker" Sleep Surface (Non-Sterile) - Taiwan Registration 7f9cdf6a55175b44e3d81fce6d636d30

Access comprehensive regulatory information for "Stryker" Sleep Surface (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 7f9cdf6a55175b44e3d81fce6d636d30 and manufactured by STRYKER MEDICAL. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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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7f9cdf6a55175b44e3d81fce6d636d30
Registration Details
Taiwan FDA Registration: 7f9cdf6a55175b44e3d81fce6d636d30
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Device Details

"Stryker" Sleep Surface (Non-Sterile)
TW: "ๅฒ่ณฝๅ…‹" ้žๅ‹•ๅŠ›ๅผๆฒป็™‚ๅบŠๅขŠ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

7f9cdf6a55175b44e3d81fce6d636d30

Ministry of Health Medical Device Import Registration No. 002524

DHA08400252408

Company Information

United States

Product Details

Has the function of supporting the patient to prevent excessive stress on the part of the body. This device can be used to treat or avoid bedsores caused by bed rest.

J General hospital and personal use equipment

J5150 Non-powered treatment mattress

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026