Taiwan FDA registration be5a99fc2c1f57c86a7de70011413a89
Gobo Brush (Unsterilized)
TW: 固博 採檢刷 (未滅菌)
Registration details
- Analysis ID
- be5a99fc2c1f57c86a7de70011413a89
- Customs Code
- DHA04400536009
Company information
- Manufacturer
- COOPER SURGICAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- FU SHING MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Sample Collection and Delivery Equipment (C.2900)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2900 Microbial sample collection and delivery equipment
- Import Information
- import
Dates and status
- Registration Date
- Nov 20, 2006
- Expiry Date
- Nov 20, 2021
- Cancellation Date
- Sep 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Gobo Brush (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number be5a99fc2c1f57c86a7de70011413a89 and manufactured by COOPER SURGICAL INC.. The authorized representative in Taiwan is FU SHING MEDICAL 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.
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