Taiwan FDA registration c85ea73da149c03050bafd29fdfec25c

"Stryker" Medical Imaging Communication Device (Non-sterilized)

TW: "史賽克" 醫學影像通訊裝置 (未滅菌)

Taiwan·Risk Class 1·STRYKER ENDOSCOPY·Registered Jun 05, 2024 – Jun 05, 2029Active

Registration details

Analysis ID: c85ea73da149c03050bafd29fdfec25c
Customs Code: DHA09402349909

Company information

Manufacturer: STRYKER ENDOSCOPY
Manufacturer Country: United States
Authorized Representative: Stryker (Far East) Co., Ltd. Taiwan Branch

Product details

Intended Use: It is limited to the first-level identification scope of the "Medical Image Communication Devices (P.2020)" and "Medical Image Storage Devices (P.2010)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): P Radiology Science
Product Type (Level 2): P.2010 Medical image storage devices;; P.2020 Medical imaging communication devices
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Jun 05, 2024
Expiry Date: Jun 05, 2029

About this record

Access comprehensive regulatory information for "Stryker" Medical Imaging Communication Device (Non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c85ea73da149c03050bafd29fdfec25c and manufactured by STRYKER ENDOSCOPY. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.

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.