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Oxygen concentrator price philips

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Commonly Used:
US$
Customization Available
Sample Available
Manufacturer First
Product Attributes:
Surgical Supplies Materials
Certification: ISO9001
Noise Level: Low
Voltage: 220V
Purity: 93.5%-94.5%
Theory: Electrotherapeutics
With LCD Display
Group: Adult
Application: Medical Institution
Scale: Medium
Material: Plastic
Ethylene Oxide Sterilization
With Logo Printing
Quality Guarantee Period: Two Years
Certification: CE
Certification: ISO13485
Purity: >94.5%

Sourcing guidance for Oxygen Concentrator Price Philips

What are the key technical specifications to evaluate when sourcing oxygen concentrators?

When comparing products like the Philips EverFlo or similar medical-grade alternatives, you must prioritize Oxygen Purity Levels, which should consistently remain between 93% ± 3%. Additionally, evaluate the Flow Rate (LPM); most home-use units range from 1 to 5 Liters Per Minute, while heavy-duty models reach 10 LPM. Ensure the device features a built-in oxygen purity sensor and an operating noise level below 45dB to ensure patient comfort and safety.

Which international compliance standards are mandatory for importing oxygen concentrators?

As medical devices, these products must adhere to strict regulatory frameworks. You must verify ISO 13485 certification for medical device quality management systems. For the US market, FDA 510(k) clearance is required, while the EU market necessitates CE Marking (MDR 2017/745). Furthermore, ensure the product meets IEC 60601-1 for electrical safety and IEC 60601-1-2 for electromagnetic compatibility.

How does the usage scenario affect the choice between stationary and portable models?

For clinical or long-term home care, stationary models (like the EverFlo) are preferred due to their continuous flow capabilities and lower maintenance needs. However, for active patients or travel, you should source Portable Oxygen Concentrators (POCs) that utilize Pulse Dose technology and are FAA-approved for airline travel. Always check the battery life (minimum 4 hours) and total weight (under 5 lbs) for portable units.

What maintenance and after-sales support should a B2B buyer expect?

Reliable suppliers should provide a warranty of at least 3 years on the compressor. Inquire about the replacement cycle for molecular sieves, which typically lasts 10,000 to 20,000 hours. Ensure the supplier offers technical training for your local engineers and maintains a steady supply of consumables like HEPA filters, nasal cannulas, and humidifier bottles.

Cross-Border Procurement & Risk Management for Medical Equipment

How can I verify the authenticity of branded products like Philips in cross-border trade?

To avoid counterfeit risks, request an Official Authorization Letter from the supplier if they claim to be a distributor. For OEM/ODM alternatives found on Made-in-China.com, verify the factory through a third-party audit (SGS or TÜV Rheinland). Always cross-reference the Unique Device Identification (UDI) numbers provided by the manufacturer with global medical databases.

What are the specific shipping precautions for oxygen concentrators?

Oxygen concentrators contain sensitive compressors and, in the case of portable units, Lithium-ion batteries, which are classified as Class 9 Dangerous Goods. You must ensure the supplier provides a Material Safety Data Sheet (MSDS) and a UN38.3 Test Report. Use reinforced wooden crate packaging to prevent vibration damage to the internal molecular sieve beds during transit.

How should I negotiate pricing and payment terms for bulk medical orders?

For orders exceeding 50 units, aim for a 15-20% volume discount. Use secure payment methods such as Letters of Credit (L/C) or Escrow services provided by reputable platforms to ensure funds are only released upon pre-shipment inspection. Avoid 100% upfront payments; a 30% deposit and 70% balance against the Bill of Lading (B/L) is the industry standard.

What are the risks regarding international trade policies for medical devices?

Be aware of import duties and medical device registration requirements in your specific country. Some regions require a Local Agent or Authorized Representative to hold the product registration. Failure to have the correct HS Code (typically 901920) and medical import license can lead to customs seizure or heavy fines.

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