Taiwan FDA registration 83a15e9b392fa9db9e95ce33cf0347a6

SKED Manual patient transfer device(Non-Sterile)

TW: "思凱得"手動病患輸送裝置(未滅菌)

Taiwan·Risk Class 1·MD·SKEDCO, INC.·Registered Oct 01, 2021 – Oct 31, 2026Active

Registration details

Analysis ID: 83a15e9b392fa9db9e95ce33cf0347a6
License Form: Ministry of Health Medical Device Import Registration No. 003597
Customs Code: DHA08400359701

Company information

Manufacturer: SKEDCO, INC.
Manufacturer Country: United States
Authorized Representative: ADEPT GENERAL CORP.

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J6785 Manual Patient Conveyor
Import Information: Imported from abroad

Dates and status

Registration Date: Oct 01, 2021
Expiry Date: Oct 31, 2026

About this record

Access comprehensive regulatory information for SKED Manual patient transfer device(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 83a15e9b392fa9db9e95ce33cf0347a6 and manufactured by SKEDCO, INC.. The authorized representative in Taiwan is ADEPT GENERAL CORP..

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