Taiwan FDA registration d873ede0883ad758d4c94e7807d4ec96
"KUMMAS" Manual Surgical Instrument for General Use (Non-Sterile)
TW: "庫瑪斯" 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·KUMMAS CORPORATION·Registered Jan 13, 2021 – Jan 13, 2026ExpiredRegistration details
- Analysis ID
- d873ede0883ad758d4c94e7807d4ec96
- License Form
- Ministry of Health Medical Device Import No. 022242
- Customs Code
- DHA09402224206
Company information
- Manufacturer
- KUMMAS CORPORATION
- Manufacturer Country
- Pakistan
- Authorized Representative
- XIANG YU INTERNATIONAL ENTERPRISE CO., LTD
Product details
- 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
Dates and status
- Registration Date
- Jan 13, 2021
- Expiry Date
- Jan 13, 2026
About this record
Access comprehensive regulatory information for "KUMMAS" 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 d873ede0883ad758d4c94e7807d4ec96 and manufactured by KUMMAS CORPORATION. The authorized representative in Taiwan is XIANG YU INTERNATIONAL ENTERPRISE CO., LTD.
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices