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"GI" SPOT ENDOSCOPIC MARKER - Taiwan Registration c6d5001f72fadb02fe0ff6d10573ae3a

Access comprehensive regulatory information for "GI" SPOT ENDOSCOPIC MARKER in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c6d5001f72fadb02fe0ff6d10573ae3a and manufactured by GI SUPPLY. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).

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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c6d5001f72fadb02fe0ff6d10573ae3a
Registration Details
Taiwan FDA Registration: c6d5001f72fadb02fe0ff6d10573ae3a
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Device Details

"GI" SPOT ENDOSCOPIC MARKER
TW: "ๅ‰ๆ„›" ๅฒๆ–‘็‰นๅ…ง่ฆ–้ก่จ˜่™Ÿๆถฒ
Risk Class 2
MD

Registration Details

c6d5001f72fadb02fe0ff6d10573ae3a

Department of Health Medical Device Import No. 011058

DHA00601105802

Company Information

Product Details

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

H Gastroenterology-urology devices

Imported from abroad

Dates and Status

Feb 22, 2005

Feb 22, 2025