Taiwan FDA registration 7a5c65caf594270f9f5c03b5ead56c5b

"PRESSURE PRODUCTS" Hemostatic Pressure Device (Non-Sterile)

TW: "普鐳休普達" 加壓止血帶 (未滅菌)

Taiwan·Risk Class 1·MD·PRESSURE PRODUCTS, INC.·Registered May 15, 2020 – May 15, 2025Expired

Registration details

Analysis ID: 7a5c65caf594270f9f5c03b5ead56c5b
License Form: Ministry of Health Medical Device Import No. 021543
Customs Code: DHA09402154302

Company information

Manufacturer: PRESSURE PRODUCTS, INC.
Manufacturer Country: United States
Authorized Representative: IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG)

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Non-inflatable Tourniquet (I.5900)".
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I5900 Non-inflatable tourniquet
Import Information: Imported from abroad

Dates and status

Registration Date: May 15, 2020
Expiry Date: May 15, 2025

About this record

Access comprehensive regulatory information for "PRESSURE PRODUCTS" Hemostatic Pressure 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 7a5c65caf594270f9f5c03b5ead56c5b and manufactured by PRESSURE PRODUCTS, INC.. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).

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