Taiwan FDA registration f88c371f96e87ef5ee97ca0dd53acf97
"Oscar" catheter guide
TW: “奧斯卡”導管導引器
Registration details
- Analysis ID
- f88c371f96e87ef5ee97ca0dd53acf97
- Customs Code
- DHA00602447105
Company information
- Manufacturer
- OSCOR INC.
- Manufacturer Country
- United States
- Authorized Representative
- TRANSMEDIC CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1340 Catheter Introducers
- Import Information
- import
Dates and status
- Registration Date
- Feb 06, 2013
- Expiry Date
- Feb 06, 2018
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Oscar" catheter guide in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f88c371f96e87ef5ee97ca0dd53acf97 and manufactured by OSCOR INC.. The authorized representative in Taiwan is TRANSMEDIC 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