Pure Global

"Termao" rod blood forceps (unsterilized) - Taiwan Registration 80e1c2098cb93e228d856c4338d25bf4

Access comprehensive regulatory information for "Termao" rod blood forceps (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 80e1c2098cb93e228d856c4338d25bf4 and manufactured by FUJINOMIYA FACTORY OF TERUMO CORPORATION;; TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
80e1c2098cb93e228d856c4338d25bf4
Registration Details
Taiwan FDA Registration: 80e1c2098cb93e228d856c4338d25bf4
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Termao" rod blood forceps (unsterilized)
TW: โ€œๆณฐ็ˆพ่Œ‚โ€ๆกฟ่ก€้‰— (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

80e1c2098cb93e228d856c4338d25bf4

DHA04400603200

Product Details

Limited to the classification and grading management of medical equipment "Blood access devices and their accessories (H.5540)" first-level identification range.

H Gastroenterology and urology

H.5540 Blood Access Devices and Accessories

import

Dates and Status

Jul 24, 2007

Jul 24, 2027