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ROSSMAX INTERNATIONAL LTD.

優盛醫學科技股份有限公司

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1988Founded
NT$831MPaid-in capital
2Plants
101Certifications
NT$1–5BRevenue band
Unified Business No.
23123644
Industry
Computers, Electronics & Optical Products (2,116)
Main products
Radiation & electro-medical equipment (120)
Location
12 F., No. 189, Gangqian Rd., Neihu Dist., Taipei City 114722, Taiwan (R.O.C.)
Taipei City (812) · Neihu Dist. (356)
Listing
Listed (TPEx) (890) 4121
Registration status
Approved / Active
Organisation type
Company Limited by Shares
Founded
1988-11-02
Paid-in capital
NT$ 831,110,450
Representative
Liu Chih-ping
Phone
(02)26597888
Website
http://www.rossmax.com
Exporter
Yes — registered with the Trade Administration
Annual revenue band
NT$1–5B
Ownership
Individually held
North American market
FDA 510(k) clearance FDA medical device registration Health Canada medical device licence
Representative tenure
In office since at least 2014 (12+ years)
Growth & profitability
Revenue 2026-09 YoY +9.2%, year-to-date +0.8%
Gross margin 33.8%, operating margin -2.5%, net margin -2% (2026-Q2 YTD)
Compliance record
FDA import refusal: 1 product(s), latest 2021-07-08
Labour Standards Act penalties: 1 case(s) in 5 years, latest 2024-06-05, fines NT$ 50,000 (Art. 24) — matched by company name

Plants 2

Certifications 101

North American market evidence 19

  • FDA 510(k) clearance K060342 2006-04-04
    ROSSMAX AUTOMATIC BLOOD PRESSURE MONITOR MODEL MO701K
  • FDA 510(k) clearance K052727 2005-12-16
    ROSSMAX NON-INVASIVE BLOOD PRESSURE MONITORS, MODELS S380, K350
  • FDA 510(k) clearance K021225 2002-05-22
    ROSSMAX AUTOMATIC BLOOD PRESSURE MONITOR, MODEL CARDIOCARE 1000I
  • FDA 510(k) clearance K013539 2002-01-17
    ROSSMAX MEDIPRO, MODELS 100F, 200F, AND 300F BLOOD PRESSURE MONITORS
  • FDA 510(k) clearance K013583 2002-01-17
    ROSSMAX MEDIPRO MODEL 10 AND 60, MEDICARE MODEL 10 AND 60 BLOOD PRESSURE MONITORS
  • FDA 510(k) clearance K011352 2001-07-20
    ROSSMAX SMARTINFLATE CARDIOPRO, MODEL 1000I AND MODEL 3000I BLOOD PRESSURE MONITORS
  • FDA 510(k) clearance K011539 2001-07-20
    ROSSMAX MEDIPRO MODEL 100, MODEL 200, AND MODEL 300 BLOOD PRESSURE MONITORS
  • FDA 510(k) clearance K011523 2001-06-14
    ROSSMAX AUTOMATIC WRISTWATCH BLOOD PRESSURE MONITOR, MODEL BPW138
  • FDA 510(k) clearance K993460 2000-01-11
    ROSSMAX AUTOMATIC WRISTWATCH BLOOD PRESSURE MONITOR, MODEL Z43
  • FDA 510(k) clearance K993426 2000-01-07
    ROSSMAX AUTOMATIC WRISTWATCH BLOOD PRESSURE MONITOR, MODEL Z44
  • FDA 510(k) clearance K993429 2000-01-07
    ROSSMAX AUTOMATIC WRISTWATCH BLOOD PRESSURE MONITOR, MODEL Z40
  • FDA 510(k) clearance K993542 1999-12-29
    ROSSMAX AUTOMATIC WRISTWATCH BLOOD PRESSURE MONITOR, MODEL V46
  • FDA 510(k) clearance K993432 1999-12-20
    ROSSMAX AUTOMATIC WRISTWATCH BLOOD PRESSURE MONITOR, MODEL Z46
  • FDA 510(k) clearance K992387 1999-08-03
    ROSSMAX AUTOMATIC WRISTWATCH BLOOD PRESSURE MONITOR, MODEL RM-4100
  • FDA 510(k) clearance K992388 1999-08-03
    ROSSMAX AUTOMATIC WRISTWATCH BLOOD PRESSURE MONITOR, MODEL RM-4200
  • FDA 510(k) clearance K964153 1998-06-11
    ROSSMAX AUTOMATIC WRISTWATCH BLOOD PRESSURE MONITOR, MODEL RM-4000
  • FDA medical device registration 9680548 2007-11-19
    System, Measurement, Blood-Pressure, Non-Invasive; Blood Pressure Cuff; Stethoscope, Manual
  • FDA import refusal 3003247551 2021-07-08
    OXIMETER, FETAL PULSE
  • Health Canada medical device licence 124160

Recent changes 1

  • Certification expiryMedical device license (Class II) certificate expired on 2026-07-15

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