Taiwan FDA registration 042277adf682adb53f7e5d135089d8a5

"Teknor" light sources and vehicles (unsterilized)

TW: "鐵克諾" 光源及載具 (未滅菌)

Taiwan·Risk Class 1·TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH.·Registered Oct 11, 2011 – Oct 11, 2021Cancelled

Registration details

Analysis ID: 042277adf682adb53f7e5d135089d8a5
Customs Code: DHA04401092400

Company information

Manufacturer: TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH.
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: Oct 11, 2011
Expiry Date: Oct 11, 2021
Cancellation Date: Oct 12, 2023

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Teknor" light sources and vehicles (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 042277adf682adb53f7e5d135089d8a5 and manufactured by TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH.. The authorized representative in Taiwan is BIOLAND ENTERPRISE INC..

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