"AbbVie" percutaneous endoscopic gastrostomy-jejunal tube group - Taiwan Registration 69b0ad79bc960f04f559a8a36dde0dcb
Access comprehensive regulatory information for "AbbVie" percutaneous endoscopic gastrostomy-jejunal tube group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 69b0ad79bc960f04f559a8a36dde0dcb and manufactured by AbbVie Deutschland GmbH & CO. KG; CLINICO MEDICAL SP. Z.O.O. BLONIE K/WROCLAWIA. The authorized representative in Taiwan is ABBVIE BIOPHARMACEUTICALS GMBH TAIWAN BRANCH (SWITZERLAND).
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Device Details
Registration Details
69b0ad79bc960f04f559a8a36dde0dcb
DHA05602992102
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
Contract manufacturing;; input
Dates and Status
Jun 28, 2017
Jun 28, 2022
Jul 01, 2022
Cancellation Information
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