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“Hologic”Specimen Radiography System - Taiwan Registration 2b9c9d0cadcc6891e6bf052afbb91ef6

Access comprehensive regulatory information for “Hologic”Specimen Radiography System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2b9c9d0cadcc6891e6bf052afbb91ef6 and manufactured by Hologic, Inc.. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

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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2b9c9d0cadcc6891e6bf052afbb91ef6
Registration Details
Taiwan FDA Registration: 2b9c9d0cadcc6891e6bf052afbb91ef6
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Device Details

“Hologic”Specimen Radiography System
TW: “豪洛捷”標本X光影像系統
Risk Class 2
MD

Registration Details

2b9c9d0cadcc6891e6bf052afbb91ef6

Ministry of Health Medical Device Import No. 035336

DHAS5603533601

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

P Radiology Science

P1680 stationary X-ray system

Imported from abroad; Consent must be attached to the input (each input must be supported by the consent of the Atomic Energy Commission)

Dates and Status

Mar 18, 2022

Mar 18, 2027