Taiwan FDA registration c8f3550bd2426290a3b895e1bf8a262d
"EMO" Truncal orthosis (Non-Sterile)
TW: "伊莫"軀幹裝具 (未滅菌)
Taiwan·Risk Class 1·MD·EMO·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- c8f3550bd2426290a3b895e1bf8a262d
- License Form
- Ministry of Health Medical Device Import Registration No. 010222
- Customs Code
- DHA08401022201
Company information
- Manufacturer
- EMO
- Manufacturer Country
- Spain
- Authorized Representative
- Heavy Maintenance Rehabilitation Products Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3490 Torso Gear
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "EMO" Truncal orthosis (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 c8f3550bd2426290a3b895e1bf8a262d and manufactured by EMO. The authorized representative in Taiwan is Heavy Maintenance Rehabilitation Products 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