Taiwan FDA registration 4c2dab2a62f08aa8a02fb64afce7c4d1
LP arm sling (unsterilized)
TW: LP手臂吊帶 (未滅菌)
Taiwan·Risk Class 1·PLUS MEDITECH CO., LTD.·Registered Dec 17, 2013 – Dec 17, 2023CancelledRegistration details
- Analysis ID
- 4c2dab2a62f08aa8a02fb64afce7c4d1
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 Physical Medical Sciences
- Product Type (Level 2)
- O.3640 手臂吊帶/醫療用三角巾
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 17, 2013
- Expiry Date
- Dec 17, 2023
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for LP arm sling (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4c2dab2a62f08aa8a02fb64afce7c4d1 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.
Free DatabasePowered by Pure Global AI89,000+ Devices