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"Siemens" diagnostic X-ray machine - Taiwan Registration 59554a7870a456444c8f11655c8bacfb

Access comprehensive regulatory information for "Siemens" diagnostic X-ray machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 59554a7870a456444c8f11655c8bacfb and manufactured by SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP. The authorized representative in Taiwan is SIEMENS LIMITED.

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including Siemens Healthcare GmbH, X-Ray Products (XP), Siemens Healthcare GmbH;; SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD., and 4 recent registrations in the same category. 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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59554a7870a456444c8f11655c8bacfb
Registration Details
Taiwan FDA Registration: 59554a7870a456444c8f11655c8bacfb
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Device Details

"Siemens" diagnostic X-ray machine
TW: โ€œ่ฅฟ้–€ๅญโ€่จบๆ–ทๅž‹Xๅ…‰ๆฉŸ
Risk Class 2
Cancelled

Registration Details

59554a7870a456444c8f11655c8bacfb

DHAS0602011204

Company Information

Product Details

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

P Radiology Science

P.1680 ๅ›บๅฎšๅผXๅ…‰็ณป็ตฑ

Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

Aug 12, 2009

Aug 12, 2019

Apr 10, 2020

Cancellation Information

Logged out

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