Taiwan FDA registration e91cdcdf3773a25dd5d698ebc6467032

"Biodenta" Orthopedic manual surgical instruments (Non-Sterile)

TW: "百丹特" 手動式骨科手術器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·BIODENTA SWISS AG·Registered Aug 27, 2013 – Aug 27, 2023Expired
Registration details
Analysis ID
e91cdcdf3773a25dd5d698ebc6467032
License Form
Ministry of Health Medical Device Import No. 013340
Customs Code
DHA09401334005
Company information
Manufacturer
BIODENTA SWISS AG
Manufacturer Country
Switzerland
Authorized Representative
Dentauspex Corporation
Product details
Intended Use
Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
Product Type (Level 1)
N Orthopedic devices
Product Type (Level 2)
N4540 Manual osteologic surgery instrument
Import Information
Imported from abroad
Dates and status
Registration Date
Aug 27, 2013
Expiry Date
Aug 27, 2023
About this record

Access comprehensive regulatory information for "Biodenta" Orthopedic manual surgical instruments (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e91cdcdf3773a25dd5d698ebc6467032 and manufactured by BIODENTA SWISS AG. The authorized representative in Taiwan is Dentauspex Corporation.

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