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"Anati" pusher (unsterilized) - Taiwan Registration 2c8021af3e4b75ae674698336e458f6b

Access comprehensive regulatory information for "Anati" pusher (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2c8021af3e4b75ae674698336e458f6b and manufactured by ANETIC AID LTD.. The authorized representative in Taiwan is JIA NAN MEDICAL INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ANETIC AID LTD, and 1 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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2c8021af3e4b75ae674698336e458f6b
Registration Details
Taiwan FDA Registration: 2c8021af3e4b75ae674698336e458f6b
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Device Details

"Anati" pusher (unsterilized)
TW: "ไบž้‚ฃๆ" ๆŽจๅบŠ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

2c8021af3e4b75ae674698336e458f6b

DHA04401217900

Company Information

United Kingdom

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Wheeled Stretcher (J.6910)".

J General hospital and personal use equipment

J.6910 Wheeled Stretcher

import

Dates and Status

Sep 18, 2012

Sep 18, 2017

Dec 20, 2019

Cancellation Information

Logged out

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