Taiwan FDA registration ec5edc8b51d51cb620ff05fe4fe637f1

"Teknor" light source and vehicle (unsterilized)

TW: "鐵克諾"光源及載具(未滅菌)

Taiwan·Risk Class 1·TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH & CO. KG·Registered May 01, 2006 – May 01, 2011Cancelled

Registration details

Analysis ID: ec5edc8b51d51cb620ff05fe4fe637f1
Customs Code: DHA04400430002

Company information

Manufacturer: TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH & CO. KG
Manufacturer Country: Germany
Authorized Representative: BIOLAND ENTERPRISE INC.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.4350 Ear, nose and throat optical fiber light sources and carriers
Import Information: import

Dates and status

Registration Date: May 01, 2006
Expiry Date: May 01, 2011
Cancellation Date: Nov 04, 2011

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for "Teknor" light source and vehicle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ec5edc8b51d51cb620ff05fe4fe637f1 and manufactured by TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH & CO. KG. The authorized representative in Taiwan is BIOLAND ENTERPRISE INC..

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