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“TRACOE” Aeris Balloon Dilation Catheter - Taiwan Registration a3b5c1fafc1829b6b2d380371a74d296

Access comprehensive regulatory information for “TRACOE” Aeris Balloon Dilation Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a3b5c1fafc1829b6b2d380371a74d296 and manufactured by TRACOE medical GmbH. The authorized representative in Taiwan is Huixing Co., 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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a3b5c1fafc1829b6b2d380371a74d296
Registration Details
Taiwan FDA Registration: a3b5c1fafc1829b6b2d380371a74d296
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Device Details

“TRACOE” Aeris Balloon Dilation Catheter
TW: “創可”艾瑞絲氣囊擴張導管
Risk Class 2
MD

Registration Details

a3b5c1fafc1829b6b2d380371a74d296

Ministry of Health Medical Device Import No. 032332

DHA05603233206

Company Information

Germany

Product Details

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

G ENT device

G4680 Bronchoscope (soft or rigid) and accessories

Imported from abroad

Dates and Status

Mar 15, 2019

Mar 15, 2024