Taiwan FDA registration ca0f238c50e136e7560ee9cec9cbc57b
OPPO Arm Sling (Non-sterile)
TW: OPPO手臂吊帶 (未滅菌)
Taiwan·Risk Class 1·MD·PLUS MEDITECH CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2024ExpiredRegistration details
- Analysis ID
- ca0f238c50e136e7560ee9cec9cbc57b
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 004909
Company information
- Manufacturer
- PLUS MEDITECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PLUS MEDITECH CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the arm sling (O.3640) of the management measures for medical equipment.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3640 arm sling
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2024
About this record
Access comprehensive regulatory information for OPPO Arm Sling (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 ca0f238c50e136e7560ee9cec9cbc57b and manufactured by PLUS MEDITECH CO., LTD.. The authorized representative in Taiwan is PLUS MEDITECH 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.
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