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Suzhou Armocon Technology Co., Ltd.

China CN-MF-000025071 Last updated 23 Oct 2026

Devices
8
Registries
EUDAMEDGUDIDFDA
FDA recalls
0

Catalogue8

  • Intimina Ref 2

    Class I EUDAMED Active
  • Intimina Ref 2

    Class I EUDAMED Active
  • Intimina Ref 2

    Class I EUDAMED Active
  • Intimina Ref 2

    Class I EUDAMED Active
  • LELO Hex Ref 4979

    Class IIb EUDAMEDFDA UDI Active
  • LELO Hex Ref 3

    Class IIb EUDAMEDFDA UDI Active
  • Intimina Ref Laselle set

    Class I EUDAMED Active
  • Intimina Ref 2

    Class I EUDAMED Active

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

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

Authorised representatives

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.

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 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.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
China
Address
77, SuHong Middle Road , suzhou, China
Website
armocon.com
PRRC contact
Shengnan Qiu
EUDAMED SRN
CN-MF-000025071
FDA FEI number
3007962592