Taiwan FDA registration fd4443eac9f117e32ae9edb1cb35d362

"OFITEL" radiographic fixture (unsterilized)

TW: “歐菲特”放射線造影固定裝置 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·ORFIT INDUSTRIES·Registered Nov 27, 2007 – Nov 27, 2022Cancelled
Registration details
Analysis ID
fd4443eac9f117e32ae9edb1cb35d362
Customs Code
DHA04400632308
Company information
Manufacturer
ORFIT INDUSTRIES
Manufacturer Country
Belgium
Product details
Intended Use
Limited to the first level recognition range of radiographic head fixator (P.1920) of the Measures for the Administration of Medical Equipment.
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1920 Head fixator for radiogram
Import Information
import
Dates and status
Registration Date
Nov 27, 2007
Expiry Date
Nov 27, 2022
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "OFITEL" radiographic fixture (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fd4443eac9f117e32ae9edb1cb35d362 and manufactured by ORFIT INDUSTRIES. The authorized representative in Taiwan is JIH FENG LUNG ENTERPRISES COMPANY LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ORFIT INDUSTRIES, 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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