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Taiwan FDA registration a837665141d8c1fe91020f322f59db50

"Creear" ear manual surgical instruments (unsterilized)　

TW: “可立耳”耳部手動式外科器械 (未滅菌)　
Taiwan flagTaiwan·Risk Class 1·COCHLEAR BONE ANCHORED SOLUTIONS AB·Registered Oct 23, 2008 – Oct 23, 2013Cancelled
Registration details
Analysis ID
a837665141d8c1fe91020f322f59db50
Customs Code
DHA04400717600
Company information
Manufacturer
COCHLEAR BONE ANCHORED SOLUTIONS AB
Manufacturer Country
Sweden
Authorized Representative
CLINICO INC.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".
Product Type (Level 1)
G ENT Science
Product Type (Level 2)
G.4420 Otolaryngology manual surgical instruments
Import Information
import
Dates and status
Registration Date
Oct 23, 2008
Expiry Date
Oct 23, 2013
Cancellation Date
Nov 15, 2016
Cancellation information
Status
Logged out
Reason
未展延而逾期者
About this record

Access comprehensive regulatory information for "Creear" ear manual surgical instruments (unsterilized)　 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a837665141d8c1fe91020f322f59db50 and manufactured by COCHLEAR BONE ANCHORED SOLUTIONS AB. The authorized representative in Taiwan is CLINICO INC..

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