Taiwan FDA registration ed10aa4130d7553be4ea5c40dc4ee7ea
"AbbVie" nasal jejunal tube
TW: “艾伯維”鼻腔空腸管
Taiwan·Risk Class 2·ABBVIE INC.;; AbbVie Ireland NL B.V.·Registered Dec 09, 2016 – Dec 09, 2021CancelledRegistration details
- Analysis ID
- ed10aa4130d7553be4ea5c40dc4ee7ea
- Customs Code
- DHA05602921100
Company information
- Manufacturer
- ABBVIE INC.;; AbbVie Ireland NL B.V.
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- ABBVIE BIOPHARMACEUTICALS GMBH TAIWAN BRANCH (SWITZERLAND)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5980 Gastric insulal tube and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Dec 09, 2016
- Expiry Date
- Dec 09, 2021
- Cancellation Date
- Dec 14, 2021
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期;;自請註銷
About this record
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).
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