Taiwan FDA registration 5c71f8201dc5b2269d8e07f85685ad0e
TestYield Second Generation Lancet (Unsterilized)
TW: 測利得 二代採血筆 (未滅菌)
Taiwan·Risk Class 1·HMD BIOMEDICAL INC.·Registered Oct 24, 2016 – Oct 24, 2026ActiveRegistration details
- Analysis ID
- 5c71f8201dc5b2269d8e07f85685ad0e
Company information
- Manufacturer
- HMD BIOMEDICAL INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HMD BIOMEDICAL INC.
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 24, 2016
- Expiry Date
- Oct 24, 2026
About this record
Access comprehensive regulatory information for TestYield Second Generation Lancet (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5c71f8201dc5b2269d8e07f85685ad0e and manufactured by HMD BIOMEDICAL INC.. The authorized representative in Taiwan is HMD BIOMEDICAL 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.
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