Across the two core clinical pathways in women's reproductive health, we offer two products already developed and registered to medical device compliance requirements, with dedicated consumables forming a complete usage loop. These two product lines are also the most important real-world data entry points for our medical data capabilities.
Addressing the full-cycle needs of women's reproductive health, we provide healthcare institutions with practical integrated solutions combining devices, consumables and data services. Select a product to open its detail page.
An innovative therapy for tubal obstructive infertility built on the principle of bio-oxidation restoring natural conception, using the strong oxidising and debriding action of ozone for integrated precise recanalisation and anti-inflammatory anti-adhesion treatment.
A non-invasive pelvic floor resonance and intelligent pelvic floor muscle activation system. Using HIFEM high-intensity focused electromagnetic fields, health is achieved while seated — covering pelvic floor training, postnatal recovery, women's intimate health and men's intimate health.
Drawing on evidence data accumulated at our core partner hospitals, we continuously capture treatment processes and efficacy indicators as reusable data assets that feed back into product development and therapy optimisation.
* The figures above are observational data compiled at the company's partner hospitals. Results vary with institution, patient population and operating standards. They do not constitute diagnostic advice or a claim of efficacy; please refer to the product registration certificate, the instructions for use and the judgement of the treating physician.
Around precise ozone control, magnetic field regulation, deep penetration and the consumable loop, we have built a complete technology chain from generation to application, and reinforced it with patents and software copyrights as an intellectual property moat.
Continuously adjustable from 15 to 65 mg/L, error ≤ ±5%, with real-time monitoring and automatic calibration.
A proprietary microwire-through technique combined with ozone intervention, delivering precise recanalisation together with anti-inflammatory and anti-adhesion effects.
1.0–5.0 T wide-range regulation with intelligent switching between low-frequency nerve stimulation and high-frequency muscle activation.
10 cm deep penetration reaching the deep pelvic floor muscles non-invasively, going beyond the 1–3 cm superficial limit of conventional approaches.
Military-grade thermal protection with a dual air-cooling system for stable 1200 W industrial-grade output.
The fallopian tube contrast catheter supports dual-phase ozone gas and liquid delivery, forming a safe and sustainable consumable loop.
A technology barrier needs both legal and systemic reinforcement: registration answers whether it can be used; patents and software copyright answer whether it is yours.
The medical ozone therapy device holds National Class II medical device registration and is qualified for nationwide market access.
An ISO quality management system covering R&D, production, inspection and after-sales service.
Multiple core patents covering ozone generation, concentration control, magnetic field regulation and catheter structure.
The control system software is copyright-registered, with integrated hardware and software keeping treatment parameters stable and controllable.
Medical Ozone Therapy Device System Control Software V1.0 · 2026SR0627822The Chinese brand "安必特" and the English brand "Armeebeauty" are both registered for Class 10 medical device goods.
安必特 No. 76761750 · Armeebeauty No. 73776559More than four years of clinical use and thousands of cases of efficacy data underpin the standardisation of the therapy and expansion of indications.
Devices and dedicated consumables are designed as a set, ensuring standardised and safe treatment, giving partners a sustainable business structure, and providing a stable standardised entry point for data collection.
Tell us your institution type and requirements and we will provide the full documentation, including product instructions, technical parameters and suitable scenarios. If your interest is clinical data collaboration, please say so directly.
