Taiwan FDA registration 74749281788851cbd87ba637bd570763

"Whitehall" Nonpowered sitz bath (Non-Sterile)

TW: "懷侯" 非動力式坐浴 (未滅菌)

Taiwan·Risk Class 1·MD·WHITEHALL MANUFACTURING, INC.·Registered Jul 04, 2016 – Jul 04, 2021Expired

Registration details

Analysis ID: 74749281788851cbd87ba637bd570763
License Form: Ministry of Health Medical Device Import No. 016734
Customs Code: DHA09401673402

Company information

Manufacturer: WHITEHALL MANUFACTURING, INC.
Manufacturer Country: United States
Authorized Representative: GOOD LINE INCORPORATION

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Sitz Bath (O.5125)".
Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O5125 Non-powered sitz bath
Import Information: Imported from abroad

Dates and status

Registration Date: Jul 04, 2016
Expiry Date: Jul 04, 2021

About this record

Access comprehensive regulatory information for "Whitehall" Nonpowered sitz bath (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 74749281788851cbd87ba637bd570763 and manufactured by WHITEHALL MANUFACTURING, INC.. The authorized representative in Taiwan is GOOD LINE INCORPORATION.

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.