Pure Global AI
Medical Device Division · registration 150178Expired

Kaneka

Hong KongCatheters, Vascular, Angioplasty, BalloonClass IVKaneka Corporation
Official record identity
MDACS listing number
150178
Model name
Fortis Catheter (R5a-8-250, R5a-8-275, R5a-8-300, R5a-8-325, R5a-8-350, R5a-8-375, R5a-8-400, R5a-13-250, R5a-13-275, R5a-13-300, R5a-13-325, R5a-13-350, R5a-13-375, R5a-13-400, R5a-13-425, R5a-13-450, R5a-18-250, R5a-18-275, R5a-18-300, R5a-18-325, R5a-18-350, R5a-18-375, R5a-18-400)
Registration date
July 07, 2015
Expiry date
July 07, 2020
Source update date
October 10, 2024
Status
Expired
Classification
Risk class
Class IV
Official value: IV
Published category
Catheters, Vascular, Angioplasty, Balloon
Published parties
Registrant / registration holder
Pacific Medical (Hong Kong) Company Limited
Official description

Catheters, Vascular, Angioplasty, Balloon

Additional source fields
AMD nomenclature code
17184
Local responsible person phone
23438009
Published manufacturer address
3-18, 2-Chome, Nakanoshima, Kita-ku, Osaka-city, Osaka, 530-8828, Japan
Published remarks
Expired.
About this record

This page mirrors one official MDACS listing. Roman-numeral classes use Hong Kong’s general medical-device scheme, while letter classes use the IVD scheme. Valid, expired, and delisted records remain distinguishable; no mixed classification scale is fabricated.