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"Hannitec" autologous blood salvage sleeve - Taiwan Registration 3c5bc7d2a200ff61a82fee6e8533ea19

Access comprehensive regulatory information for "Hannitec" autologous blood salvage sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3c5bc7d2a200ff61a82fee6e8533ea19 and manufactured by Haemonetics Mexico Manufacturing S. de R.L. de C.V. The authorized representative in Taiwan is HAEMONETICS ASIA INCORPORATED TAIWAN BRANCH (U.S.A.).

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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3c5bc7d2a200ff61a82fee6e8533ea19
Registration Details
Taiwan FDA Registration: 3c5bc7d2a200ff61a82fee6e8533ea19
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Device Details

"Hannitec" autologous blood salvage sleeve
TW: "ๆผขๅฐผๅธๅ…‹" ่‡ช้ซ”่ก€ๆถฒๅ›žๆ”ถ็ฎกๅฅ—
Risk Class 2
Cancelled

Registration Details

3c5bc7d2a200ff61a82fee6e8533ea19

DHA00601120706

Product Details

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

D Anesthesiology

import

Dates and Status

Apr 19, 2005

Apr 19, 2020

Jun 16, 2022

Cancellation Information

Logged out

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