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Designed for US hospitals, wound‑care centers, and sports‑medicine clinics seeking reliable pressure therapy at a competitive price.
Get Free Quote in 24 h1. Escalating Treatment Costs – US hospitals report a 12% annual rise in hyperbaric therapy expenses, squeezing margins.
2. Patient Demand for Faster Recovery – Studies show a 30% reduction in wound‑healing time when therapy is delivered at 2.0 ATA compared with 1.5 ATA.
3. Regulatory Pressure – CMS and FDA audits increasingly require documented compliance (CE, FDA, ISO 9001) for all pressure‑vessel equipment.
4. Supply‑Chain Bottlenecks – Relying on a single overseas supplier can add 6‑8 weeks to lead times, jeopardizing scheduling.
| Parameter | Specification |
|---|---|
| Operating Pressure | 2.0 ATA ±0.05 ATA |
| Chamber Volume | 150 L (standard); customizable up to 300 L |
| Material | AISI 316L stainless steel, 3‑layer anti‑corrosion coating |
| Power Supply | 220‑240 V, 50/60 Hz, 2 kW |
| Control System | Touch‑screen PLC, ISO‑compliant alarm hierarchy |
| Safety Certifications | CE, FDA 21 CFR 820, ISO 13485, CB, RoHS, VDE |
| Warranty | 24 months parts & labor |
hyperbaric-chamber-2-ata hyperbaric-chamber
Q1: What is the typical lead time for a 2.0 ATA hyperbaric chamber shipped to the USA?
A: Standard ex‑works production is 28 days; with DDP shipping to a US port, total delivery averages 35‑40 days.
Q2: Can the chamber be customized for specific patient‑monitoring interfaces?
A: Yes. Our OEM/ODM service supports custom PLC programming, integration with existing hospital information systems, and branding of the control console.
Q3: How does the chamber meet FDA 21 CFR 820 requirements?
A: All units undergo FDA‑registered design controls, traceable component sourcing, and full documentation packages, including Design History File (DHF) and Device Master Record (DMR).
Q4: What after‑sales support is included?

A: 24 / 7 technical hotline, on‑site installation training (up to 2 days), and a 24‑month warranty covering parts, labor, and software updates.
Q5: Are there financing or leasing options for US buyers?
A: We partner with accredited financial institutions to offer up‑front purchase, lease‑to‑own, and equipment‑as‑a‑service (EaaS) models.
Q6: How is the chamber shipped to comply with hazardous‑material regulations?
A: Each unit is classified as a non‑hazardous pressure vessel and packed in ISO‑compliant wooden crates with UN‑type marking for safe transport.
Q7: Does the chamber support 24‑hour continuous operation?
A: Yes. Our cooling system and redundant safety valves allow uninterrupted therapy cycles, validated for 72‑hour continuous use.
Q8: What documentation is provided for procurement?
A: Full set of CE Declaration of Conformity, FDA 510(k) summary, ISO certificates, test reports, and a detailed user manual (English).
Limited‑time offer: **Free 30‑day trial unit** for qualified US hospitals + complimentary installation training.
Request Your Free Quote NowOr call us directly at +1 (800) 555‑0199 (US toll‑free) – Available 24 h.
Laura Mitchell, Procurement Manager – Mercy Hospital
“The price was 22% below our previous vendor, and the chamber passed FDA audit on first inspection. Delivery was on schedule, saving us a critical two‑week delay.”
James Patel, Clinical Engineer – Boston Medical Center
“Installation was finished in one day, and the integrated monitoring dashboard synced with our EMR without any extra coding.”
Rebecca Lee, Director of Rehabilitation – Seattle Sports Institute
“Our athletes have reported faster recovery, and the OEM branding helped us differentiate our service offerings.”
Trusted By Leading Healthcare Providers
Certificates: CE, FDA 510(k), ISO 9001, ISO 13485, RoHS, VDE, CB, GS, SAA, HACCP/GMP, IPPC.