Taiwan FDA registration cf7e1ffbcd0e6df5b5d9e34c378e66dd

"Philips" diagnostic X-ray tube sleeve assembly (unsterilized)

TW: “飛利浦”診斷用X光球管套組件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·PHILIPS MEDICAL SYSTEMS DMC GMBH·Registered Jun 21, 2013 – Jun 21, 2018Cancelled
Registration details
Analysis ID
cf7e1ffbcd0e6df5b5d9e34c378e66dd
Customs Code
DHAS4401313009
Company information
Manufacturer Country
Germany
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
Limited to the first-level identification range of the Measures for the Administration of Medical Devices "X-ray Tube Sleeve Components for Diagnosis (P.1760)".
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1760 診斷用X光球管套組件
Import Information
Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
Registration Date
Jun 21, 2013
Expiry Date
Jun 21, 2018
Cancellation Date
Dec 13, 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 "Philips" diagnostic X-ray tube sleeve assembly (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cf7e1ffbcd0e6df5b5d9e34c378e66dd and manufactured by PHILIPS MEDICAL SYSTEMS DMC GMBH. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including PHILIPS MEDICAL SYSTEMS DMC GMBH, GILARDONI S.P.A., and 5 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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