Taiwan FDA registration 376b6a212ec05aab95425dad50b9f314
"Retina" X-ray film for medical use
TW: "瑞蒂納" 醫療用X光軟片
Taiwan·Risk Class 1·CARESTREAM HEALTH, INC.·Registered Oct 27, 2005 – Oct 27, 2010CancelledRegistration details
- Analysis ID
- 376b6a212ec05aab95425dad50b9f314
- Customs Code
- DHA04400133006
Company information
- Manufacturer
- CARESTREAM HEALTH, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Kangshi Medical Equipment Co., Ltd
Product details
- Intended Use
- A radioactive transparent sheet material, covered with a single or double-sided emulsion of a photographic film, which can be used to record images during diagnostic radiology.
- Product Type (Level 1)
- P Radiology Science
- Import Information
- import
Dates and status
- Registration Date
- Oct 27, 2005
- Expiry Date
- Oct 27, 2010
- Cancellation Date
- Jan 17, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Retina" X-ray film for medical use in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 376b6a212ec05aab95425dad50b9f314 and manufactured by CARESTREAM HEALTH, INC.. The authorized representative in Taiwan is Taiwan Kangshi Medical Equipment 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