Taiwan FDA registration 7b1e3dfd9f9eba0498861293d39b02fb

"Synthes" Orthopedic Manual Surgical Instrument (NON-STERILE)

TW: "新社思" 手動式骨科手術器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·SYNTHES (USA)·Registered Nov 23, 2015 – Nov 23, 2020Cancelled
Registration details
Analysis ID
7b1e3dfd9f9eba0498861293d39b02fb
License Form
Ministry of Health Medical Device Import No. 015882
Customs Code
DHA09401588202
Company information
Manufacturer
SYNTHES (USA)
Manufacturer Country
United States
Authorized Representative
PRO-READY ENTERPRISE CO., LTD.
Product details
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
Nov 23, 2015
Expiry Date
Nov 23, 2020
Cancellation Date
Jun 16, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期未申請展延
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About this record

Access comprehensive regulatory information for "Synthes" 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 7b1e3dfd9f9eba0498861293d39b02fb and manufactured by SYNTHES (USA). The authorized representative in Taiwan is PRO-READY ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including AVALIGN TECHNOLOGIES, and 1 recent registrations in the same category. 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.

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