ALMAG-01 Portable PEMF Therapy Device — 4-Emitter Traveling Magnetic Field System

Connect the four coil emitters to the main control unit using the included cables. Arrange the coils in a line along the target area — for example, along the length of a leg, across the lower back, or surrounding a joint. The coils should lie flat against or alongside the body surface. Turn on the control unit to begin the traveling field sequence. Sessions typically run 10–20 minutes, and the auto-shutoff timer ends the session automatically. No active monitoring is required once the device is running. Refer to the included instruction manual for placement guidance specific to different areas of the body.

Most users begin with daily sessions for the first 2–3 weeks, then move to 3–5 sessions per week as a maintenance protocol. Consistency produces better results than session length — a short daily session typically outperforms infrequent longer sessions. If you have a specific wellness goal, discuss session frequency with your healthcare provider, who can advise based on your individual circumstances.

Individual responses vary significantly. Some users report noticing a difference in how they feel within the first week of consistent use. Others describe gradual changes over 2–4 weeks of regular sessions. The research behind the ELAMED traveling field protocol reflects outcomes from sustained, consistent use rather than single sessions. We encourage a 30-day consistent trial before drawing conclusions. Results are not guaranteed and depend on the individual, their health status, session frequency, and the area being addressed.

The ALMAG-01 can be used on most major areas of the body — limbs, joints, the back, shoulders, and neck are the most common application sites. The four coils are designed to run sequentially along an area, so they work particularly well across longer muscle groups and joints with surrounding tissue. The device should not be used directly over implanted electronic devices, and should not be applied to the abdomen during pregnancy. See the Contraindications section on this page for the complete exclusion list, and refer to the instruction manual for guidance on specific body areas.

The ALMAG-01 is contraindicated for individuals with pacemakers, implanted cardioverter-defibrillators (ICDs), cochlear implants, insulin pumps, or any other active implanted electronic device. It is also contraindicated during pregnancy, in the presence of active hemorrhage, for individuals with active malignancies, systemic blood diseases, thyrotoxicosis, severe cardiac conditions, or during acute inflammatory episodes or fever. If any of these conditions apply, do not use this device without explicit physician clearance. If you have a health condition not listed here and are uncertain whether PEMF use is appropriate, consult your healthcare provider before purchasing or beginning use.

All four Almagia devices share ELAMED manufacturing heritage and CE Class IIa certification. The key differences are protocol complexity and intended use. The ALMAG-01 uses a single traveling field protocol at a fixed 6 pps frequency — straightforward setup, no mode selection, designed for reliable home use by people new to PEMF. The ALMAG+ adds multiple frequency modes and program options for users who want more protocol flexibility. The MAGOFON-01 adds vibroacoustic therapy (vibration combined with PEMF) for more specialized joint and localized tissue applications. The ALMAG-02 offers 79 preset programs and a field strength range of 2–45 mT, making it the professional and clinical-grade option in the lineup. See the comparison table on this page for a full side-by-side breakdown.

CE Class IIa is a European medical device classification under the Medical Device Directive (MDD 93/42/EEC). Class IIa devices are medium-risk medical devices — a category that includes devices intended to interact with the human body for diagnostic or therapeutic purposes. Achieving CE Class IIa certification requires demonstrating the device meets specific safety and performance standards, including documentation of clinical evidence, technical design files, and manufacturer quality system requirements. For PEMF devices, this classification reflects a recognized standard of regulatory review that is meaningfully different from a device with no certification at all. The ALMAG-01 is CE Class IIa certified. We make no FDA registration, clearance, or approval claims of any kind.

Many people use PEMF devices alongside their regular medications without issue, but we recommend consulting your prescribing physician or pharmacist before beginning use if you take any prescription medications — particularly anticoagulants, cardiac medications, thyroid medications, or medications that affect circulation or nerve function. PEMF is not a treatment and does not replace medication. Your healthcare provider is the appropriate person to advise on any potential interactions with your specific medication regimen.

The ALMAG-01 comes with a 1-year manufacturer warranty from ELAMED covering manufacturing defects and device malfunctions under normal use conditions. If you experience a hardware issue within the warranty period, contact our support team at (888) 500-5675 or reach out through our website. Recovery Room Direct is an authorized dealer of Almagia International products, which means warranty service is backed by the manufacturer and supported by our team. Physical damage, misuse, or use outside of the device's specified parameters are not covered by the manufacturer warranty.

Free parcel shipping is available to addresses in the contiguous 48 states. Shipping to Alaska, Hawaii, US territories, or international destinations may be available but requires a shipping quote. Contact us at (888) 500-5675 before placing your order if you are located outside the contiguous US and we will confirm availability and any associated shipping costs.

We accept returns on the ALMAG-01 within 30 days of delivery for items in original, unused condition with all original packaging and components. A 20% restocking fee applies to all returned devices. Return shipping costs are the responsibility of the buyer. Devices that have been used, damaged, or returned without original packaging may not be eligible for a full refund. To initiate a return, contact our team at (888) 500-5675 — we will provide return instructions and a return authorization number.

Yes — Affirm financing is available at checkout on qualifying orders. Affirm offers 0% APR options and payment plans ranging from 3 to 24 months, depending on your creditworthiness and the plan selected at checkout. Affirm financing is subject to a credit check and approval by Affirm. Current terms, available plan lengths, and APR options are displayed during checkout. HSA/FSA payment may also be accepted — check with your benefits administrator, and ask your healthcare provider about a Letter of Medical Necessity if you plan to use those funds. This does not constitute tax or medical advice.

Yes. Recovery Room Direct is an authorized dealer of Almagia International products, including the ALMAG-01. Purchasing from an authorized dealer means your device is a genuine ELAMED-manufactured product, your warranty is valid and manufacturer-backed, and you have access to our recovery specialists for setup support and any questions that come up after delivery. We do not sell third-party refurbished or gray-market units — every Almagia device we ship is new, factory-sealed, and backed by the 1-year manufacturer warranty.