Taiwan FDA registration f24c6bb4f047aeaee500b031c645d372
“IZI” Osteo-Site Bone Biopsy Needle Set (Sterile)
TW: “埃利埃”骨活檢針(滅菌)
Registration details
- Analysis ID
- f24c6bb4f047aeaee500b031c645d372
- License Form
- Ministry of Health Medical Device Import No. 035749
- Customs Code
- DHA05603574902
Company information
- Manufacturer
- IZI MEDICAL PRODUCTS, LLC
- Manufacturer Country
- United States
- Authorized Representative
- HONEST MEDICAL EQUIPMENT MACAU COMPANY LIMITED TAIWAN BRANCH (MACAU)
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H1075 Gastroenterology - Urology biopsy instruments
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 18, 2022
- Expiry Date
- Aug 18, 2027
About this record
Access comprehensive regulatory information for “IZI” Osteo-Site Bone Biopsy Needle Set (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f24c6bb4f047aeaee500b031c645d372 and manufactured by IZI MEDICAL PRODUCTS, LLC. The authorized representative in Taiwan is HONEST MEDICAL EQUIPMENT MACAU COMPANY LIMITED TAIWAN BRANCH (MACAU).
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