Taiwan FDA registration 5e3c8fb02341be42844949682d4d6f50

Ytterbium Titanium Manual Orthopedic Surgical Instrument Set (Unsterilized)

TW: "鐿鈦"手動式骨科手術器械組 (未滅菌)

Taiwan·Risk Class 1·INTAI TECHNOLOGY CORP.·Registered Apr 25, 2006 – Apr 25, 2016Cancelled

Registration details

Analysis ID: 5e3c8fb02341be42844949682d4d6f50

Company information

Manufacturer: INTAI TECHNOLOGY CORP.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: INTAI TECHNOLOGY CORP.

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 Orthopedics
Product Type (Level 2): N.4540 手動式骨科手術器械
Import Information: Domestic

Dates and status

Registration Date: Apr 25, 2006
Expiry Date: Apr 25, 2016
Cancellation Date: Jun 26, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Ytterbium Titanium Manual Orthopedic Surgical Instrument Set (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5e3c8fb02341be42844949682d4d6f50 and manufactured by INTAI TECHNOLOGY CORP.. The authorized representative in Taiwan is INTAI TECHNOLOGY CORP..

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.