Taiwan FDA registration 62d23eed60d2b720368d19219d90ff37

Schweimei diagnostic X-ray tube sleeve assembly (unsterilized)

TW: "史威邁" 診斷用X光球管套組件 (未滅菌)

Taiwan·Risk Class 1·SWEMAC MEDICAL APPLIANCES AB·Registered Sep 20, 2016 – Sep 20, 2021Cancelled

Registration details

Analysis ID: 62d23eed60d2b720368d19219d90ff37
Customs Code: DHAS9401701802

Company information

Manufacturer: SWEMAC MEDICAL APPLIANCES AB
Manufacturer Country: Sweden
Authorized Representative: GREENEVER MEDICAL SYSTEMS INC .

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: Sep 20, 2016
Expiry Date: Sep 20, 2021
Cancellation Date: Sep 23, 2023

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for Schweimei 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 62d23eed60d2b720368d19219d90ff37 and manufactured by SWEMAC MEDICAL APPLIANCES AB. The authorized representative in Taiwan is GREENEVER MEDICAL SYSTEMS INC ..

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