ALMAG-02 Professional PEMF Therapy System — 79 Programs, 3 Emitters, 20cm Depth

The ALMAG-02 ships with four coil emitters that are placed on or near the target area of the body. For most applications, the coils are positioned along the limb or body region and secured in place during the session. The professional instruction manual included with the unit provides detailed coil placement diagrams for various application types and program numbers.

Session duration depends on the selected program. Each of the 79 preset programs includes a recommended duration. For manual mode, typical session lengths range from 15 to 30 minutes. The built-in auto-shutoff timer ends the session automatically — no need to watch the clock. Start with lower-intensity programs when beginning and work up as comfortable over the first few weeks of use.

Most protocols in the clinical PEMF research literature suggest daily or near-daily use for the first four to six weeks, then maintenance use of three to five times per week. The ALMAG-02’s 79-program library includes protocols designed for both intensive and maintenance use phases.

Because the ALMAG-02 is a professional device with adjustable parameters, we recommend following the program guidance in the included manual and discussing a specific schedule with your healthcare provider, particularly if you are managing a health condition.

PEMF device outcomes vary by individual, application area, frequency of use, and the programs selected. Many users report noticing changes within the first two to four weeks of consistent daily use. Research on PEMF technology generally notes that effects are cumulative — more consistent protocols over longer periods tend to produce more noticeable changes than sporadic use.

The ALMAG-02 is not a treatment device and does not diagnose or cure any condition. It is designed to support the body’s natural recovery and wellness processes. Individual results are not guaranteed.

The ALMAG-02 and its four coil emitters may be positioned along the limbs, back, shoulders, hips, and other body regions as described in the instruction manual. The device is designed to support general wellness, circulation support, and recovery applications.

Do not apply the coils over the head or directly over the heart. Do not apply to the throat or thyroid region. Avoid direct application over implanted electronic devices. The full instruction manual provides specific guidance for safe placement across different application types.

If you have any of the following conditions, do not use the ALMAG-02 without explicit guidance from your healthcare provider: pacemakers or other implanted electronic devices, pregnancy, active hemorrhage or bleeding disorders, malignancies, systemic blood diseases, severe cardiac conditions, thyrotoxicosis, or acute inflammatory conditions.

For users with other chronic conditions or who are taking prescription medications, consult your healthcare provider before beginning any PEMF protocol. This is particularly important for cardiovascular conditions, as the ALMAG-02 operates at field strengths up to 45 mT — higher than many consumer PEMF devices.

The ALMAG-01 is a single-mode traveling PEMF device with a fixed 6 pps frequency and up to 25 mT field strength — ideal for first-time PEMF users who want a simple, proven protocol. The ALMAG+ adds multi-mode capability and multiple preset programs while maintaining up to 25 mT field strength. The MAGOFON-01 combines vibroacoustic therapy with PEMF in a single-pad form factor for joint-focused applications.

The ALMAG-02 is the flagship unit: 79 preset programs, full 1–100 pps frequency adjustment, 2–45 mT field strength adjustment, and dual-mode traveling and stationary operation. It is the most capable device in the line, designed for practitioners and advanced home users who need clinical-level parameter control.

CE Class IIa is a European medical device regulatory classification under the Medical Device Directive (MDD 93/42/EEC). Class IIa devices are considered medium-risk medical devices that require conformity assessment by a notified body before they can be CE marked and sold in European markets.

For the ALMAG-02, CE Class IIa certification means the device has been assessed against relevant safety and performance standards, including ISO 13485:2016 for quality management in medical device manufacturing. ELAMED®, the manufacturer, has over 40 years of medical device manufacturing history. CE Class IIa is the appropriate certification standard for PEMF therapeutic devices of this type.

CE certification is a European standard. The ALMAG-02 is sold in the United States as a wellness device.

Consult your prescribing healthcare provider before combining PEMF device use with any prescription medication, particularly blood thinners, cardiovascular medications, or medications that affect circulation. The ALMAG-02 is designed to support circulation and tissue recovery — effects that may interact with certain medication protocols.

Do not use the device in a way that conflicts with your healthcare provider’s instructions. The ALMAG-02 is not a medical treatment device and does not replace medical care or prescription therapy.

The ALMAG-02 comes with a 1-year manufacturer warranty from ELAMED® covering defects in materials and workmanship under normal use. As an authorized dealer, Recovery Room Direct supports warranty claims for products purchased through our store.

If you experience any issue with your unit within the warranty period, contact us at (888) 500-5675 and our PEMF support team will coordinate the resolution process with you directly.

At this time, Recovery Room Direct ships the ALMAG-02 within the contiguous 48 United States only. We are not currently able to ship to Alaska, Hawaii, US territories, or international destinations. The free shipping offer applies to the contiguous 48 states.

If you are located outside the contiguous US and have questions about your options, please call us at (888) 500-5675.

We accept returns on the ALMAG-02 within 30 days of delivery for units in original, unused condition in original packaging. Returns are subject to a 20% restocking fee, and the buyer is responsible for return shipping costs. Units that have been used, are missing components, or show signs of damage are not eligible for return.

To initiate a return, contact our team at (888) 500-5675 before shipping anything back. We will provide return authorization and instructions.

Yes. Affirm financing is available at checkout for qualified buyers. Affirm offers installment payment plans that allow you to spread the investment over time. Select Affirm at payment during checkout to view available terms and check your eligibility. Affirm financing is subject to Affirm’s own credit approval process and terms. Orders must meet minimum qualifying amounts, which are displayed at checkout.

HSA and FSA funds may also be used for this purchase with a Letter of Medical Necessity from a qualifying healthcare provider. Consult your plan administrator for eligibility — this is not tax advice.

Yes. Recovery Room Direct is an authorized dealer of Almagia International products, including the ALMAG-02. Purchasing through an authorized dealer ensures you receive a genuine CE Class IIa certified unit, valid manufacturer warranty coverage, and access to manufacturer support through our team. We do not sell gray-market, refurbished, or third-party units.