Taiwan FDA registration 946483ab85a6c680672e878e7c612325

"Team Power" SUCTION BAG (Non-Sterile)

TW: "勤達" 廢液收集袋 (未滅菌)

Taiwan·Risk Class 1·MD·HOSPITECH MANUFACTURING SERVICES SDN BHD·Registered Oct 29, 2014 – Oct 29, 2024Expired

Registration details

Analysis ID: 946483ab85a6c680672e878e7c612325
License Form: Ministry of Health Medical Device Import No. 014616
Customs Code: DHA09401461602

Company information

Manufacturer: HOSPITECH MANUFACTURING SERVICES SDN BHD
Manufacturer Country: Malaysia
Authorized Representative: TEAM POWER MEDICAL INSTRUMENT LTD.

Product details

Intended Use: Limited to the first level of identification scope of "non-powered, single-patient, portable suction device (I.4680)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I4680 Non-powered, single-patient, portable suction device
Import Information: Imported from abroad

Dates and status

Registration Date: Oct 29, 2014
Expiry Date: Oct 29, 2024

About this record

Access comprehensive regulatory information for "Team Power" SUCTION BAG (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 946483ab85a6c680672e878e7c612325 and manufactured by HOSPITECH MANUFACTURING SERVICES SDN BHD. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT 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.