"Guofa" restraint belt (unsterilized)
Taiwan·Risk Class 1·K.F. MEDICAL INSTRUMENTS CO., LTD.·Registered Oct 20, 2005 – Oct 20, 2015Cancelled- Analysis ID
- 4f76b020ce2fe545c82484df5f8c3b46
- Customs Code
- DHY04300043600
- Manufacturer
- K.F. MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- K.F. MEDICAL INSTRUMENTS CO., LTD.
- Intended Use
- For the purpose of restricting the movement of the patient during treatment or examination and to protect the patient or others due to medical necessity.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6760 保護性限制帶
- Import Information
- Domestic
- Registration Date
- Oct 20, 2005
- Expiry Date
- Oct 20, 2015
- Cancellation Date
- Apr 25, 2018
- Status
- Logged out
- Reason
- 自行鍵入
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Access comprehensive regulatory information for "Guofa" restraint belt (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4f76b020ce2fe545c82484df5f8c3b46 and manufactured by K.F. MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is K.F. MEDICAL INSTRUMENTS CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including K.F. MEDICAL INSTRUMENTS CO., LTD., 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.