HENYO MEDICAL DEVICE CATALOG

HENYO 10 L/min Oxygen Concentrator

Review the HENYO 10 L/min Oxygen Concentrator as its own HENYO medical-device configuration, then confirm prescribed flow, destination-market requirements, electrical supply, accessories, exact-model documentation, warranty, and service plan.

SKU: HY-OC-ST-10L-SF
Category: Respiratory Equipment
Brand: HENYO
Supply support: Model review, device documentation, export packing and service planning

REQUEST INFORMATION

BUILD YOUR REQUIREMENT

Choose size, quantity, and specification path.

Use this planning tool to prepare an inquiry. Availability, final pack quantities, pricing, production, freight, and the signed specification are confirmed by HENYO TECARE in writing.

Electrical configuration

110 V · 60 HzDestination plug confirmed before production220 V · 50 HzDestination plug confirmed before productionDestination reviewVoltage, frequency and plug checked by HENYO

Quantity format

UnitsIndividual HENYO concentrator quantityCasesOne protected export unit per case, subject to final packingPalletsUnit count and freight plan confirmed by quotation

Quantity

1 units · approximately 1 pieces

SELECTED REQUIREMENTHENYO 10 L/min Oxygen Concentrator · 110 V · 60 Hz · 1 UnitsSKU HY-OC-ST-10L-SF

Request this configuration

HENYO MEDICAL DEVICE TECHNICAL DATA

PRODUCT SPECIFICATION SHEET

SKUHY-OC-ST-10L-SF

ProductHENYO 10 L/min Oxygen Concentrator

Device formatStationary continuous-flow oxygen concentrator with one flowmeter and digital control display

Rated oxygen flow0–10 L/min target; the signed model specification controls the usable adjustment range

Oxygen concentration target93% ±3% at rated flow; verify with the approved model-specific performance report

Outlet pressure target20–60 kPa; confirm the exact production configuration

Power-supply optionsAC 220 V ±22 V, 50 Hz ±1 Hz or AC 110 V ±11 V, 60 Hz ±1 Hz; destination plug and rating confirmed by order

Input-power target800 VA maximum planning value; confirm the nameplate and signed specification

Sound-pressure target50 dB(A) or lower under the stated test conditions; verify the model-specific report

Nominal dimensions344 × 306 × 565 mm

Nominal net weight20 kg

InterfaceSingle flowmeter, digital display, timing and voice-capable control layout shown; final enabled functions confirmed by model

HumidificationTop-mounted humidifier-bottle configuration shown; supplied bottle and connection confirmed by packing list

NebulizationOptional atomization configuration, target ≥0.15 mL/min, only when separately quoted and documented

Alarm reviewConfirm power-failure, low-oxygen, pressure, temperature, and service alarms for the exact model

Standard-accessory reviewConfirm nasal cannula, humidifier bottle, filters, power cord, instructions, and warranty documentation

Clinical-use boundarySupplemental oxygen is used only as prescribed and supervised; this device is not represented here as life-supporting or patient-monitoring equipment

Destination-market evidenceBefore sale or import, verify exact-model authorization, labeling, ISO 80601-2-69 evidence, IEC 60601 electrical-safety and EMC evidence, breathing-gas-path evaluation, warranty, and qualified service support

MEDICAL-DEVICE BUYER APPROVAL CHECKLIST

Before ordering or importing the selected model, confirm the documents and services required for the intended market:

Signed model-specific specification, approved sample, label, instructions for use, and accessories list
Destination-market establishment and device authorization or registration evidence where applicable
Electrical-safety, electromagnetic-compatibility, oxygen-performance, alarm, and reliability evidence for the exact model
Rated voltage, frequency, plug, environmental limits, warranty, spare-parts plan, and qualified service support
Approved export packaging, serial and lot traceability, inspection record, and shipping documentation

Medical-device specification notice: These are HENYO target purchasing specifications for model selection and quotation. They are not an authorization, certification, prescription, or model-specific test report. Final claims, intended use, configuration, and destination-market status must match the signed specification and current supporting documents for the exact device supplied.