Is this your brand? Sign in to claim ownership.
Sign in to claim this brandSHENZHEN AEON TECHNOLOGY CO., LTD.
China·CN-MF-000012690
Last updated May 30, 2026
What SHENZHEN AEON TECHNOLOGY CO., LTD. makes
Shenzhen Aeon Technology produces disposable and reusable pulse oximeters for monitoring blood oxygen saturation and heart rate, infrared skin thermometers for measuring body temperature, compressor nebulizers for inhaling liquid medication, and transcutaneous electrical nerve stimulation (TENS) units for pain relief.
The company’s devices are classified as Class II and Class IIa under EU and FDA regulations, with listings in the EUDAMED and FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in China.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Shenzhen Aeon Technology Co., Ltd. manufacture?
Shenzhen Aeon Technology Co., Ltd. specializes in devices for patient monitoring and therapy, including disposable and reusable pulse oximeters (for measuring blood oxygen saturation and heart rate), infrared skin thermometers (for body temperature monitoring), compressor nebulizers (for delivering inhaled medications), and TENS/EMS units (for pain relief via electrical stimulation). These devices cater to clinical and home-use settings.
Where is Shenzhen Aeon Technology Co., Ltd. based, and how does that affect its devices?
The company is headquartered in China. While the country of origin does not inherently determine regulatory classification or compliance, its devices are designed to meet international standards like those of the EU (Class II/IIa) and the FDA (Class II/IIa), ensuring they can be registered in global databases such as EUDAMED and the FDA’s UDI system.
Which regulatory registries list Shenzhen Aeon Technology Co., Ltd.’s devices?
The company’s devices are listed in two key regulatory databases: EUDAMED, the European Union’s medical device registry, and the FDA’s Unique Device Identifier (UDI) database, which tracks devices authorized in the U.S. These listings help healthcare providers and regulators verify compliance and traceability for Class II/IIa devices.
How are Shenzhen Aeon Technology Co., Ltd.’s devices classified under EU and FDA regulations?
The company’s devices fall under Class II and Class IIa classifications in both the EU and FDA frameworks. This classification is based on their intended use—for example, pulse oximeters and nebulizers are considered higher-risk due to their role in critical monitoring or therapy, requiring stricter regulatory oversight and compliance with specific safety and performance standards.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- China
- Address
- 808 XinBaoYi Industrial Bld., Hou Ting Village Bei Ting Rd., Shajing baoan, shenzhen Guangdong, China
- Website
- www.szastec.com
- —
- —
- [email protected]
- Phone
- +86 755 25030234
- PRRC Contact
- ciny Wu
- EUDAMED SRN
- CN-MF-000012690
- FDA FEI Number
- —
- DUNS Number
- 529372064
Catalogue (553)
Page 3 of 12| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Kg Physio | U80B | FDA UDI | Class II | Active |
| Alphamed | U80EH | FDA UDI | Class II | Active |
| Muifa | U80BH | FDA UDI | Class II | Active |
| Abox | U80H | FDA UDI | Class II | Active |
| Alphamed | U81Q | FDA UDI | Class II | Active |
| Aeon | A330N | FDA UDI | Class II | Active |
| AlphagoMed | U80K | FDA UDI | Class II | Active |
| DrKumo | U80M | FDA UDI | Class II | Active |
| AlphaMed | U60A | FDA UDI | Class II | Active |
| Auvon | AS8012C | FDA UDI | Class II | Active |
| The Doc In A Box | U62I | FDA UDI | Class II | Active |
| Nursal | AS1080 | FDA UDI | Class II | Active |
| Ampmed | U81QH | FDA UDI | Class II | Active |
| Juning | U80AH | FDA UDI | Class II | Active |
| BeeGoline | U60AH | FDA UDI | Class II | Active |
| Eeslrnoe | U80AH | FDA UDI | Class II | Active |
| AlphaMed | UFR109 | FDA UDI | Class II | Active |
| Sdunw | U80A | FDA UDI | Class II | Active |
| AlphagoMed | U81H | FDA UDI | Class II | Active |
| Ulaif | U80LH | FDA UDI | Class II | Active |
| Auvon | AS8012 | FDA UDI | Class II | Active |
| Vicsainteck | AS1080-A55 | FDA UDI | Class II | Active |
| Medicpad | AS1080 | FDA UDI | Class II | Unknown |
| Vibeey | UFR101 | FDA UDI | Class II | Active |
| Teyiyes | U80U | FDA UDI | Class II | Active |
| Guaever | U60B | FDA UDI | Class II | Active |
| carda health | U82W | FDA UDI | Class II | Active |
| AlphaMed | U80AH | FDA UDI | Class II | Active |
| Hylogy® | U80AH | FDA UDI | Class II | Active |
| Andesfit Health | U60AH | FDA UDI | Class II | Active |
| Tec.bean | AS1080 | FDA UDI | Class II | Active |
| Urion | U60BH | FDA UDI | Class II | Active |
| MedLine systems | U80EH | FDA UDI | Class II | Active |
| Urion | U62GH | FDA UDI | Class II | Active |
| Aeon | A310B | FDA UDI | Class II | Unknown |
| AlphagoMed | U80T | FDA UDI | Class II | Active |
| Tovendor | U60EH | FDA UDI | Class II | Active |
| Auvon | AS8012C | FDA UDI | Class II | Active |
| Auvon | AS1080 | FDA UDI | Class II | Active |
| Aeon | A330B | FDA UDI | Class II | Unknown |
| KAI Lifestyle&Wellness | UFR102 | FDA UDI | Class II | Active |
| Aoeom | UFR101 | FDA UDI | Class II | Active |
| Auvon | AS1080 | FDA UDI | Class II | Active |
| firhealth | U60AH | FDA UDI | Class II | Active |
| AlphaMed | U80Y | FDA UDI | Class II | Active |
| Andesfit Health | U80BH | FDA UDI | Class II | Active |
| Alphamed | U85H | FDA UDI | Class II | Active |
| Aeon | A340L | FDA UDI | Class II | Active |
| Elera | U81E | FDA UDI | Class II | Active |
| Pur-Well Living | U80EH | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.