Taiwan FDA registration 5ca762a8a017045194abc5e8e29c67a5

"Teknort" manual instruments for general surgery (unsterilized)

TW: “鐵克諾”一般手術用手動式器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH & CO. KG·Registered Jun 26, 2006 – Jun 26, 2011Cancelled
Registration details
Analysis ID
5ca762a8a017045194abc5e8e29c67a5
Customs Code
DHA04400478602
Company information
Manufacturer Country
Germany
Authorized Representative
BIOLAND ENTERPRISE INC.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4800 Hand Instruments for General Surgery
Import Information
import
Dates and status
Registration Date
Jun 26, 2006
Expiry Date
Jun 26, 2011
Cancellation Date
Nov 30, 2012
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Teknort" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5ca762a8a017045194abc5e8e29c67a5 and manufactured by TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH & CO. KG. The authorized representative in Taiwan is BIOLAND ENTERPRISE INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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