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"Tessy" alternating pressure mattress (unsterilized) - Taiwan Registration 38a0e94c85d5cb550fb8bff2d1e5e981

Access comprehensive regulatory information for "Tessy" alternating pressure mattress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 38a0e94c85d5cb550fb8bff2d1e5e981 and manufactured by THE SURGICAL COMPANY INTERNATIONAL B. V.. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE 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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38a0e94c85d5cb550fb8bff2d1e5e981
Registration Details
Taiwan FDA Registration: 38a0e94c85d5cb550fb8bff2d1e5e981
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Device Details

"Tessy" alternating pressure mattress (unsterilized)
TW: โ€œๆณฐๅธŒโ€ไบคๆ›ฟๅผๅฃ“ๅŠ›ๆฐฃๅขŠๅบŠ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

38a0e94c85d5cb550fb8bff2d1e5e981

DHA04401172203

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Alternating Pressure Air Mattress (J.5550)".

J General hospital and personal use equipment

J.5550 ไบคๆ›ฟๅผๅฃ“ๅŠ›ๆฐฃๅขŠๅบŠ

import

Dates and Status

May 18, 2012

May 18, 2022

Apr 12, 2024

Cancellation Information

Logged out

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