"Teknort" manual instruments for general surgery (unsterilized)
- Analysis ID
- 5ca762a8a017045194abc5e8e29c67a5
- Customs Code
- DHA04400478602
- Manufacturer
- TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- BIOLAND ENTERPRISE INC.
- 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
- Registration Date
- Jun 26, 2006
- Expiry Date
- Jun 26, 2011
- Cancellation Date
- Nov 30, 2012
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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.