Taiwan FDA registration 0ba6951a29cc9db03a3e5ded62602bbe
Greenever Light Beam Patient Position Indicator (Non-Sterile)
TW: 常捷 病患定位光束指示器 (未滅菌)
Taiwan·Risk Class 1·MD·CEDAR ELECTRO INC.·Registered Aug 23, 2018 – Aug 23, 2023ExpiredRegistration details
- Analysis ID
- 0ba6951a29cc9db03a3e5ded62602bbe
- License Form
- Ministry of Health Medical Device Import No. 019540
- Customs Code
- DHA09401954004
Company information
- Manufacturer
- CEDAR ELECTRO INC.
- Manufacturer Country
- Canada
- Authorized Representative
- GREENEVER MEDICAL SYSTEMS INC .
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Equipment "Patient Positioning Beam Indicator (P.5780)".
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P5780 Patient Positioning Beam Indicator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 23, 2018
- Expiry Date
- Aug 23, 2023
About this record
Access comprehensive regulatory information for Greenever Light Beam Patient Position Indicator (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 0ba6951a29cc9db03a3e5ded62602bbe and manufactured by CEDAR ELECTRO INC.. The authorized representative in Taiwan is GREENEVER MEDICAL SYSTEMS INC ..
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