Taiwan FDA registration e6c2c53a7d5ba0c36178dd98ae88f775

"Guanya" spine manual surgical instruments (unsterilized)

TW: “冠亞”脊椎手動式手術用器械 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Guanya International Technology Co., Ltd. Taipei Factory·Registered Apr 11, 2012 – Apr 11, 2017Cancelled
Registration details
Analysis ID
e6c2c53a7d5ba0c36178dd98ae88f775
Company information
Manufacturer Country
Taiwan, Province of China
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 11, 2012
Expiry Date
Apr 11, 2017
Cancellation Date
Nov 28, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Guanya" spine manual surgical instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e6c2c53a7d5ba0c36178dd98ae88f775 and manufactured by Guanya International Technology Co., Ltd. Taipei Factory. The authorized representative in Taiwan is Guanya International Technology Co., Ltd. Taipei Factory.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TOPASIA INTERNATIONAL TECHNOLOGY INC., 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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