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"Minimally invasive" foreign body forceps - Taiwan Registration 1e12f069136bde5594e743d344be5741

Access comprehensive regulatory information for "Minimally invasive" foreign body forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1e12f069136bde5594e743d344be5741 and manufactured by Micro-Tech (Nanjing) Co., Ltd.. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE 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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1e12f069136bde5594e743d344be5741
Registration Details
Taiwan FDA Registration: 1e12f069136bde5594e743d344be5741
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Device Details

"Minimally invasive" foreign body forceps
TW: โ€œๅพฎๅ‰ตโ€็•ฐ็‰ฉ้‰—
Risk Class 2
Cancelled

Registration Details

1e12f069136bde5594e743d344be5741

DHA09200082900

Company Information

Product Details

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

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

Chinese goods;; input

Dates and Status

Jul 25, 2017

Jul 25, 2022

Apr 12, 2024

Cancellation Information

Logged out

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