Suzhou Armocon Technology Co., Ltd.
China CN-MF-000025071 Last updated 23 Oct 2026
- Devices
- 8
- Registries
- EUDAMEDGUDIDFDA
- FDA recalls
- 0
Catalogue
EUDAMED certificates
TÜV Rheinland LGA Products GmbH 0197 1 certificate
- HZ 2155884-1 Issued
Quality management system EU MDR
- Issued
- 1 Apr 2026
- Expires
- 31 Mar 2031
Related companies
Authorised representatives
- LELOi AB SE
Notified bodies
What Suzhou Armocon Technology Co., Ltd. makes
Suzhou Armocon Technology Co., Ltd. manufactures personal wellness devices, including vaginal trainers and sexual health products such as the INTIMINA line and the LELO Hex, a wearable stimulation device.
These products are classified under EU medical device regulations as Class I or Class IIb and are registered in the EU’s eudamed database. The company is based in China.
Frequently asked questions
What types of medical devices does Suzhou Armocon Technology Co., Ltd. manufacture?
Suzhou Armocon Technology Co., Ltd. specializes in personal wellness devices focused on sexual health and intimate wellness. Their product line includes vaginal trainers and wearable stimulation devices, such as the INTIMINA range and the LELO Hex. These devices are designed to support physical training and sensory stimulation in a personal wellness context.
Where is Suzhou Armocon Technology Co., Ltd. based?
The company is headquartered in Suzhou, China. This location serves as its primary operational base for manufacturing and distributing its wellness devices.
Are Suzhou Armocon Technology Co., Ltd.’s devices listed in any regulatory registries?
Yes, Suzhou Armocon Technology Co., Ltd.’s devices are registered in the eudamed database, which is the European Union’s central registry for medical devices. This listing ensures transparency and compliance with EU regulatory requirements for medical devices.
How are Suzhou Armocon Technology Co., Ltd.’s devices classified under EU medical device regulations?
Under EU medical device regulations, Suzhou Armocon Technology Co., Ltd.’s devices fall into Class I or Class IIb classifications. The classification depends on factors like intended use, risk level, and interaction with the body. Class IIb indicates a higher-risk category requiring stricter regulatory oversight, while Class I devices are generally considered lower risk.
Information
- Country
- China
- Address
- 77, SuHong Middle Road , suzhou, China
- Website
- armocon.com
- [email protected]
- PRRC contact
- Shengnan Qiu
- EUDAMED SRN
- CN-MF-000025071
- FDA FEI number
- 3007962592