Manufacturer · Germany

HBOT Chambers & Systems from Dremenia Sauerstofftechnik

Manufacturer claims only
Dremenia Sauerstofftechnik hyperbaric oxygen chamber
At a Glance

Dremenia Sauerstofftechnik is a German chamber manufacturer headquartered in Haiger that offers all three chamber categories - soft-sided, monoplace and multiplace - for 1 to 6 occupants at 1.3 to 2.0 ATA, serving the DACH region and the wider EU. Every certification documented for this profile - CE conformity, a DHZ hygiene certificate and TUV-tested components - is a statement from the manufacturer's own website; as of 22 July 2026 our records contain no register-verified certification for this company.

Key Facts
Chamber TypesSoft-sided, Monoplace, Multiplace
Operating Pressure1.3-2.0 ATA
Capacity1-6 persons
Price RangeNot publicly listed
Service AreaDACH/EU, Europe-wide delivery; HQ Haiger, Germany
Installation & MaintenanceEurope-wide delivery; optional on-site assembly and instruction; service packages incl. TPU aging measurement; spare parts
WarrantyStatutory warranty; optional packages up to 10 years
B2B ReferencesARARAT Grand Residences, ANTI Berlin, The Biohacking Club München, IUNE Medical Center, OXYTHEA Düsseldorf
Company

Company & Products

Dremenia Sauerstofftechnik operates from its headquarters in Haiger, Germany, with partner locations across Germany, Austria and Switzerland. The documented lineup covers soft-sided chambers, monoplace steel chambers and multiplace steel chambers, with capacities ranging from 1 to 6 persons.

Operating pressure spans 1.3 to 2.0 ATA across the range. Note that the manufacturer's own pages disagree on the upper limit: the about-us FAQ caps steel chambers at 2.0 ATA, while the homepage and the HyperOxy Prestige product page mention up to 2.5 ATA - the latter only as a custom build by prior arrangement. This profile conservatively lists 2.0 ATA, which the HyperOxy Ultra multiplace confirms as its maximum working pressure.

Certifications

Certifications & Verification Status

Dremenia states CE conformity with applicable EU directives, a DHZ hygiene certificate, and TUV-tested components on selected models. All three claims come from the company's own website (retrieved 22 July 2026) and are marked manufacturer-stated in our records.

As of the research date, no register-verified certification is documented for Dremenia - our dossier records no register entry for this company, and no ISO 13485 claim appears in the sources we reviewed. Buyers planning medical or clinical use should request notified-body documentation and declarations of conformity directly from the manufacturer before purchase.

Service

Service, Warranty & Support

Delivery is Europe-wide by freight forwarder, with optional on-site assembly and user instruction. Maintenance and service packages include TPU aging measurement and are also offered for third-party chambers - a notable option for operators with mixed fleets. Support is German-language, and spare parts shipping is offered.

On warranty, Dremenia offers the statutory warranty plus optional, individually configurable warranty packages with terms of up to 10 years. The stated service area is DACH and the EU.

Fit

References & Who It Suits

The manufacturer lists five B2B reference installations: ARARAT Grand Residences, ANTI Berlin, The Biohacking Club Muenchen, IUNE Medical Center and OXYTHEA Duesseldorf. These names come from the company's own project page; they are not independently verified, and the sources do not document what kind of facility each one is.

The documented range - three chamber categories, 1 to 6 occupants, 1.3 to 2.0 ATA overall - spans single-user setups through group operation. The sources do not map specific chamber types to pressure levels or intended settings, so buyers should confirm per-model specifications directly with the manufacturer. The EU-wide delivery and German-language support make the offer most practical for buyers in the DACH region and neighboring EU markets.

Verified Data

Every data point on this profile is source-checked. Certifications are only marked as verified when confirmed in official registers - never on manufacturer claims alone.

Sources we verify against
  • FDA 510(k) database
  • EUDAMED registry
  • Manufacturer filings