Taiwan FDA registration c724b4f28cec18e3abd795369c76762f

"SCHINDLER" Surgical camera and accessories (Non-Sterile)

TW: "辛德勒" 外科手術用照相機及其附件 (未滅菌)

Taiwan·Risk Class 1·MD·SCHINDLER ENDOSKOPIE TECHNOLOGIE GMBH·Registered Feb 19, 2020 – Feb 19, 2025Expired

Registration details

Analysis ID: c724b4f28cec18e3abd795369c76762f
License Form: Ministry of Health Medical Device Import No. 021294
Customs Code: DHA09402129407

Company information

Manufacturer: SCHINDLER ENDOSKOPIE TECHNOLOGIE GMBH
Manufacturer Country: Germany
Authorized Representative: SMARTECH MEDICAL CO., LTD.

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Surgical Cameras and Their Accessories (I.4160)".
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I4160 Surgical Camera and Its Accessories
Import Information: Imported from abroad

Dates and status

Registration Date: Feb 19, 2020
Expiry Date: Feb 19, 2025

About this record

Access comprehensive regulatory information for "SCHINDLER" Surgical camera and accessories (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c724b4f28cec18e3abd795369c76762f and manufactured by SCHINDLER ENDOSKOPIE TECHNOLOGIE GMBH. The authorized representative in Taiwan is SMARTECH MEDICAL CO., LTD..

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