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Baxter International BAX Reportable Segment — European Medical Devices Regulation

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Other financials

Income statement

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Revenue$2.7B+2.9%
Gross profit$891.0M+3.5%
Operating income$66.0M+13.8%
Net income-$15.0M-112%
EPS (diluted)-$0.03-112%

Balance sheet

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Cash & equivalents$2.0B-12.1%
Total debt$224.0M-8.9%
Total equity$6.0B-14.7%
Total assets$19.8B-6.8%

Cash flow

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Operating cash flow$213.0M+210%
CapEx$128.3M+15.0%
Free cash flow$83.0M-42.1%

Valuation

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Market cap$10.27B-50.6%
Enterprise value$8.48B-55.6%
P/S0.9×-1.0×

Profitability

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Gross margin30.1%-5.9pp
Operating margin-2.7%
Net margin-9.7%+62.5pp
FCF margin3%-2.4pp

Returns & leverage

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Return on equity-16.7%-76.7pp
Debt / equity0.0×
Current ratio1.9×-0.2×

Where this comes from

Reported directly by Baxter International in its filing.

Tagged under the XBRL concept bax:EuropeanMedicalDevicesRegulationExpenses.

The official record: Baxter International’s 10-K, filed February 12, 2026, on SEC EDGAR. View the filing →

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Questions, answered.

What is Baxter International's reportable segment — european medical devices regulation?
Baxter International (BAX) reported reportable segment — european medical devices regulation of -$5.25M in Q4 2025.
How has Baxter International's reportable segment — european medical devices regulation changed year-over-year?
Baxter International's reportable segment — european medical devices regulation increased by 36.4% year-over-year, from -$8.25M to -$5.25M.
What is the long-term trend for Baxter International's reportable segment — european medical devices regulation?
Over 3 years (2022 to 2025), Baxter International's reportable segment — european medical devices regulation has grown at a -20.6% compound annual growth rate (CAGR), from -$42M to -$21M.
What does reportable segment — european medical devices regulation mean?
Costs incurred to comply with European Union medical device safety and regulatory standards.
How do you interpret reportable segment — european medical devices regulation?
High costs reflect the regulatory burden of maintaining market access; a decrease suggests the completion of major compliance phases.
How does reportable segment — european medical devices regulation compare across companies?
Comparable to 'Regulatory Compliance Costs' or 'Legal/Regulatory Remediation' for medical device companies operating in Europe.