Taiwan FDA registration e2e0904ce30e7c0d24fb05a0a063541e
"Libao" inspection brush (sterilized/unsterilized)
TW: “立寶”採檢刷(滅菌/未滅菌)
Taiwan·Risk Class 1·Taiwan Libao Medical Equipment Co., Ltd·Registered Aug 28, 2012 – Aug 28, 2027ActiveRegistration details
- Analysis ID
- e2e0904ce30e7c0d24fb05a0a063541e
Company information
- Manufacturer
- Taiwan Libao Medical Equipment Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LIBO MEDICAL PRODUCTS INC.
Product details
- Intended Use
- Limited to the classification and grading management measures for medical equipment "Microbial Sample Collection and Delivery Equipment (C.2900)" the first level identification range.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2900 Microbial sample collection and delivery equipment
- Import Information
- Domestic
Dates and status
- Registration Date
- Aug 28, 2012
- Expiry Date
- Aug 28, 2027
About this record
Access comprehensive regulatory information for "Libao" inspection brush (sterilized/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e2e0904ce30e7c0d24fb05a0a063541e and manufactured by Taiwan Libao Medical Equipment Co., Ltd. The authorized representative in Taiwan is LIBO MEDICAL PRODUCTS INC..
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