Taiwan FDA registration b3e4cbc834791faca8637508e6d4bced

"Fubi" manual osteologic surgical instrument (unsterilized)

TW: "普美" 手動式骨科手術器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·PRO-MED INSTRUMENTE GMBH·Registered Mar 14, 2006 – Mar 14, 2011Cancelled
Registration details
Analysis ID
b3e4cbc834791faca8637508e6d4bced
Customs Code
DHA04400294002
Company information
Manufacturer Country
Germany
Authorized Representative
WONDERFUL INSTRUMENTS COMPANY, LTD.
Product details
Intended Use
Manual orthopedic surgical instruments are hand-held devices that can cut tissue or can be used in combination with other equipment in orthopedic surgery.
Product Type (Level 1)
N Orthopedics
Product Type (Level 2)
N.4540 手動式骨科手術器械
Import Information
import
Dates and status
Registration Date
Mar 14, 2006
Expiry Date
Mar 14, 2011
Cancellation Date
Jan 18, 2013
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Fubi" manual osteologic surgical instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b3e4cbc834791faca8637508e6d4bced and manufactured by PRO-MED INSTRUMENTE GMBH. The authorized representative in Taiwan is WONDERFUL INSTRUMENTS COMPANY, 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.

Free DatabasePowered by Pure Global AI89,000+ Devices