"Teknort" manual instruments for general surgery (unsterilized)
Taiwan·Risk Class 1·TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH.·Registered Jul 04, 2011 – Jul 04, 2021Cancelled- Analysis ID
- 8643a64c697b4a5412dfbbcc95ec7fa5
- Customs Code
- DHA04401053308
- Manufacturer
- TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH.
- Manufacturer Country
- Germany
- Authorized Representative
- BIOLAND ENTERPRISE INC.
- Intended Use
- Limited to the first level identification scope 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
- Jul 04, 2011
- Expiry Date
- Jul 04, 2021
- Cancellation Date
- Oct 12, 2023
- Status
- Logged out
- Reason
- 未展延而逾期者
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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 8643a64c697b4a5412dfbbcc95ec7fa5 and manufactured by TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH.. 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 & CO. KG, 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.