Taiwan FDA registration 70ebce36af4bdbe6728fe8c351a957ab
"Baxter" volthemagglutination endoscope is catheterized
TW: “百特”伏血凝內視鏡應用導管
Taiwan·Risk Class 2·BAXTER HEALTHCARE CORPORATION·Registered Jun 10, 2011 – Jun 10, 2016CancelledRegistration details
- Analysis ID
- 70ebce36af4bdbe6728fe8c351a957ab
- Customs Code
- DHA00602243606
Company information
- Manufacturer
- BAXTER HEALTHCARE CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- BAXTER HEALTHCARE LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Jun 10, 2011
- Expiry Date
- Jun 10, 2016
- Cancellation Date
- May 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Baxter" volthemagglutination endoscope is catheterized in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 70ebce36af4bdbe6728fe8c351a957ab and manufactured by BAXTER HEALTHCARE CORPORATION. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..
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