Taiwan FDA registration 4aaee5355dcc4219c8f02b33898ab5df

"Airp" Medical Sealed Injection Source (Unsterilized)

TW: "艾爾普" 醫用密封射源 (未滅菌)

Taiwan·Risk Class 1·ISOTOPE PRODUCTS LABORATORIES·Registered Apr 13, 2006 – Apr 13, 2016Cancelled

Registration details

Analysis ID: 4aaee5355dcc4219c8f02b33898ab5df
Customs Code: DHAS4400372801

Company information

Manufacturer: ISOTOPE PRODUCTS LABORATORIES
Manufacturer Country: United States
Authorized Representative: GLOBAL MEDICAL SOLUTIONS TAIWAN, LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Nuclear Medical Seal Calibration Source (P.1400)".
Product Type (Level 1): P Radiology Science
Product Type (Level 2): P.1400 醫用密封校正射源
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: Apr 13, 2006
Expiry Date: Apr 13, 2016
Cancellation Date: Apr 25, 2018

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Airp" Medical Sealed Injection Source (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4aaee5355dcc4219c8f02b33898ab5df and manufactured by ISOTOPE PRODUCTS LABORATORIES. The authorized representative in Taiwan is GLOBAL MEDICAL SOLUTIONS TAIWAN, LTD..

This page provides complete technical specifications, regulatory compliance details. 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.