Taiwan FDA registration 2bae5e251bc16cdc5a7e4170aa4fd1bd

"Hanmo" inflatable tourniquet (unsterilized)

TW: “涵莫”充氣式止血帶(未滅菌)

Taiwan·Risk Class 1·HAMMARPLAST MEDICAL AB·Registered Dec 25, 2012 – Dec 25, 2022Cancelled

Registration details

Analysis ID: 2bae5e251bc16cdc5a7e4170aa4fd1bd
Customs Code: DHA04401252101

Company information

Manufacturer: HAMMARPLAST MEDICAL AB
Manufacturer Country: Sweden
Authorized Representative: MEDISOL ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Inflatable Tourniquet (I.5910)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.5910 充氣式止血帶
Import Information: import

Dates and status

Registration Date: Dec 25, 2012
Expiry Date: Dec 25, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Hanmo" inflatable tourniquet (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2bae5e251bc16cdc5a7e4170aa4fd1bd and manufactured by HAMMARPLAST MEDICAL AB. The authorized representative in Taiwan is MEDISOL ENTERPRISE CO., LTD..

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