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Battery portable oxygen concentrator

I have found results from3000+products and1000+suppliers aboutBattery portable oxygen concentrator

Commonly Used:
US$
Customization Available
Sample Available
Manufacturer First
Product Attributes:
Application: Medical Institution
Scale: Medium
Voltage: 220V
Medical Device Regulatory Type: Type 2
Customized: Non-Customized
Certification: CE
Noise Level: Low
Physiological Functions of Diagnosis and Monitoring Equipment
Application: Home
Scale: Small
Voltage: 380V
Certification: FDA
Certification: EEC
Certification: ISO13485
Certification: ISO9001

Sourcing guidance for Battery Portable Oxygen Concentrator

What are the key technical specifications to prioritize when sourcing a Battery Portable Oxygen Concentrator?

Buyers must focus on Oxygen Concentration Purity, which should be 93% ± 3% to meet medical standards. Additionally, evaluate the Pulse Flow vs. Continuous Flow settings; pulse flow is more common for portable units to conserve battery. Ensure the device utilizes High-Quality Molecular Sieves (preferably imported) for stable oxygen production and has a Noise Level below 45dB for user comfort.

How should battery performance and portability be evaluated for B2B procurement?

Prioritize units with Lithium-ion batteries that offer at least 4-8 hours of duration at a setting of 2. Check for Dual Power Options (AC/DC) and FAA Approval if the target market includes air travelers. The total weight should ideally be under 5 lbs (2.3 kg) for true portability, and the unit should include a custom-fit carrying bag with proper ventilation to prevent overheating.

What international compliance standards are mandatory for this category?

As a medical device, it must adhere to ISO 13485 (Quality Management Systems for Medical Devices). For the US market, FDA 510(k) clearance is essential; for the EU, CE Marking (MDR 2017/745) is required. Additionally, ensure the battery components have UN38.3 certification to comply with international dangerous goods shipping regulations.

What are the maintenance requirements and after-sales expectations for POCs?

Suppliers should provide User-Replaceable Filters and clear indicators for Sieve Bed Replacement. B2B buyers should negotiate a warranty of at least 2-3 years on the main unit and 6-12 months on batteries. Demand a technical support response time of <24 hours and verify if the supplier provides video tutorials for troubleshooting and maintenance.

Cross-Border Purchasing & Risk Mitigation for Medical Devices

What are the specific risks associated with shipping battery-powered medical devices internationally?

The primary risk involves Lithium Battery Regulations. POCs are classified as Class 9 Dangerous Goods if the battery exceeds certain Watt-hour limits. You must ensure the supplier provides a Material Safety Data Sheet (MSDS) and a Safe Transport Report. Failure to provide correct labeling can lead to customs seizures or heavy fines at the port of entry.

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

Look for 'Audited Suppliers' who have undergone on-site inspections by third-party agencies like SGS or TÜV Rheinland. Check their Export Experience specifically in the medical sector and request Product Test Reports that match the factory name. Using Secured Trading Services on Made-in-China.com is highly recommended to protect your payment until the goods pass quality inspection.

What negotiation strategies should be used for bulk POC orders?

Negotiate based on Tiered Pricing; for example, a 15-20% discount for orders exceeding 100 units. Instead of just focusing on the unit price, negotiate for extra consumables (filters, nasal cannulas) or extended battery warranties to be included in the package. Request a Pre-Shipment Inspection (PSI) clause in the contract to ensure every unit meets the specified oxygen purity levels before leaving the factory.

How do I handle customs clearance for medical equipment in different regions?

Ensure the supplier provides a Commercial Invoice with accurate HS Codes (typically 901920). For the US, you may need an Initial Importer Registration with the FDA. Always confirm that the Product Labeling and User Manuals are in the local language of the destination country, as this is a frequent cause for Customs Holds during the clearance process.

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