"MAXER" Manual surgical instrument for general use (Non-sterile)
- Analysis ID
- c99511aaa01227370db735aa6ae9ebd3
- License Form
- Ministry of Health Medical Device Import No. 015879
- Customs Code
- DHA09401587900
- Manufacturer
- MAXER ENDOSCOPY GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- REVO LASER CORPORATION
- 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 and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
- Registration Date
- Nov 20, 2015
- Expiry Date
- Nov 20, 2025
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Access comprehensive regulatory information for "MAXER" Manual surgical instrument for general use (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c99511aaa01227370db735aa6ae9ebd3 and manufactured by MAXER ENDOSCOPY GMBH. The authorized representative in Taiwan is REVO LASER CORPORATION.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MAXER MEDIZINTECHNIK 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.