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Small oxygen concentrator

I have found results from10000+products and4000+suppliers aboutSmall oxygen concentrator

Commonly Used:
US$
Customization Available
Sample Available
Manufacturer First
Product Attributes:
Type: Breathing Apparatus
Application: Home
Scale: Medium
Voltage: 220V
Certification: ISO9001
Noise Level: Low
Purity: 93.5%-94.5%
Function: Biological Regulatio
Theory: Electrotherapeutics
With LCD Display
Group: Adult
Customized: Non-Customized
Purpose: Gas Manufacturing
Application Fields: Electronic
Condition: New
Application: Medical Institution
Scale: Small
Scale: Large
Voltage: 110V
Certification: RoHS
Certification: CE
Certification: ISO13485
Certification: ISO
Noise Level: Ultra Low
Purity: >94.5%

Sourcing guidance for Small Oxygen Concentrator

What are the key technical specifications to consider when selecting a small oxygen concentrator?

Buyers must prioritize Oxygen Concentration Levels, which should ideally be 93% ± 3% at all flow settings for medical-grade use. Pay close attention to the Flow Rate (L/min); small units typically range from 1L to 5L. Additionally, evaluate the Noise Level, ensuring it is below 45dB for home or bedside use, and verify the Molecular Sieve life expectancy, which should exceed 10,000 hours of operation.

Which international compliance standards are mandatory for this product category?

As a medical device, the product must adhere to ISO 13485 (Medical Devices Quality Management Systems). For the US market, FDA 510(k) clearance is essential, while the EU market requires CE Marking (MDR 2017/745). Furthermore, ensure the device meets IEC 60601-1 for basic safety and essential performance of medical electrical equipment.

How does the portability and power system affect the usage scenarios?

For 'Small' or 'Portable' units, the Battery Life is critical; look for a minimum of 3-4 hours of runtime. The unit should support AC/DC power auto-switching, allowing it to be used in vehicles (12V car adapters) and during international travel. The total weight should ideally be under 5kg for true portability in travel or outdoor scenarios.

What maintenance requirements should B2B buyers communicate to their end-users?

The design should feature User-Replaceable Filters (HEPA and intake filters) to reduce long-term service costs. Suppliers should provide a clear Maintenance Schedule, typically involving cleaning the filter every 100 hours and replacing it every 6-12 months. Units with Self-Diagnostic Alarms for low oxygen purity or power failure are highly preferred for safety.

Cross-Border Procurement & Risk Management for Medical Devices

How can I verify the credibility of a medical device supplier on Made-in-China.com?

Always look for Audited Suppliers who have undergone third-party verification by agencies like SGS or TÜV Rheinland. Request their Medical Device Production License and check if they have a proven track record of exporting to your target region. You can also use the Secured Trading Service on Made-in-China.com to ensure payment safety until the goods are verified.

What are the common risks in shipping oxygen concentrators internationally?

The primary risk involves Lithium Battery Regulations if the unit is portable; these are classified as Class 9 Dangerous Goods, requiring specific labeling and UN38.3 certification. For stationary units, ensure the Compressor is secured with transit bolts to prevent internal damage from vibrations during sea or air freight.

What negotiation strategies should be used for bulk medical equipment orders?

Focus on Warranty Extensions and Spare Parts Kits (e.g., extra molecular sieves or compressors) rather than just the unit price. Negotiate for OEM/ODM branding at lower MOQs if you are building a private label. Request a Pre-shipment Inspection (PSI) clause in the contract to ensure the oxygen purity of the actual batch meets the agreed specifications.

How should I handle customs clearance for medical-grade oxygen concentrators?

Ensure the HS Code (typically 901920) is correctly declared. You must provide the Declaration of Conformity, Commercial Invoice, and Packing List that matches the medical registrations in the destination country. Failure to provide a valid Import License for medical devices can lead to immediate seizure by customs.

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