Taiwan FDA registration 8cfb61321f0c3db1b618d56ac5b49552

"Centinel Spine" Orthopedic manual surgical instrument (Non-Sterile)

TW: “伸特耐-脊椎”手動式骨科手術器械 (未滅菌)

Taiwan·Risk Class 1·MD·Centinel Spine, LLC·Registered May 25, 2020 – May 25, 2025Expired

Registration details

Analysis ID: 8cfb61321f0c3db1b618d56ac5b49552
License Form: Ministry of Health Medical Device Import No. 021568
Customs Code: DHA09402156805

Company information

Manufacturer: Centinel Spine, LLC
Manufacturer Country: United States
Authorized Representative: RACK MEDICAL TECHNOLOGIES, INC.

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: May 25, 2020
Expiry Date: May 25, 2025

About this record

Access comprehensive regulatory information for "Centinel Spine" Orthopedic manual surgical instrument (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 8cfb61321f0c3db1b618d56ac5b49552 and manufactured by Centinel Spine, LLC. The authorized representative in Taiwan is RACK MEDICAL TECHNOLOGIES, 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.