Taiwan FDA registration 7fe80d8a63c26d7bb79f396ff83cfdab
"Foro" dental X-ray (unsterilized)
TW: "福羅"牙科用X光片 (未滅菌)
Registration details
- Analysis ID
- 7fe80d8a63c26d7bb79f396ff83cfdab
- Customs Code
- DHA04400231005
Company information
- Manufacturer
- FLOW X-RAY CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- SE-US CO., LTD.
Product details
- Intended Use
- Radiographic films are made of radioactive transparent flakes of material covered with a single- or double-sided image emulsion, which can be then used to record images during diagnosis.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1840 Radiographic film
- Import Information
- import
Dates and status
- Registration Date
- Dec 22, 2005
- Expiry Date
- Dec 22, 2025
About this record
Access comprehensive regulatory information for "Foro" dental X-ray (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7fe80d8a63c26d7bb79f396ff83cfdab and manufactured by FLOW X-RAY CORPORATION. The authorized representative in Taiwan is SE-US 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