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"AbbVie" nasal jejunal tube - Taiwan Registration ed10aa4130d7553be4ea5c40dc4ee7ea

Access comprehensive regulatory information for "AbbVie" nasal jejunal tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ed10aa4130d7553be4ea5c40dc4ee7ea and manufactured by ABBVIE INC.;; AbbVie Ireland NL B.V.. The authorized representative in Taiwan is ABBVIE BIOPHARMACEUTICALS GMBH TAIWAN BRANCH (SWITZERLAND).

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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ed10aa4130d7553be4ea5c40dc4ee7ea
Registration Details
Taiwan FDA Registration: ed10aa4130d7553be4ea5c40dc4ee7ea
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Device Details

"AbbVie" nasal jejunal tube
TW: โ€œ่‰พไผฏ็ถญโ€้ผป่…”็ฉบ่…ธ็ฎก
Risk Class 2
Cancelled

Registration Details

ed10aa4130d7553be4ea5c40dc4ee7ea

DHA05602921100

Company Information

Product Details

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

H Gastroenterology and urology

H.5980 Gastric insulal tube and its accessories

import

Dates and Status

Dec 09, 2016

Dec 09, 2021

Dec 14, 2021

Cancellation Information

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