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Sign in to claim this brandDongguan Aimei Silicone Products Co., Ltd.
US
Last updated May 23, 2026
What Dongguan Aimei Silicone Products Co., Ltd. makes
The company produces reusable menstrual cups and discs made from non-latex silicone, designed for menstrual hygiene management. These products are intended for single-user, long-term use and are marketed under multiple variants, including the AneerCare line and bassrose.
The portfolio consists of Class II medical devices, authorised under the FDA’s Unique Device Identification (UDI) system. These products are listed in the FDA’s UDI database, adhering to U.S. regulatory requirements for Class II devices. The company operates from the United States.
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 Dongguan Aimei Silicone Products Co., Ltd. manufacture?
The company specializes in reusable menstrual cups and discs made from non-latex silicone. These products are designed for menstrual hygiene management and are intended for single-user, long-term use. The portfolio includes multiple variants under the AneerCare brand and the bassrose line.
Where is Dongguan Aimei Silicone Products Co., Ltd. based?
The company operates from the United States, though its name suggests origins in Dongguan, China. The manufacturing and regulatory focus align with U.S. standards, including compliance with the FDA’s Unique Device Identification (UDI) system.
Which regulatory registries list the company’s devices?
The company’s menstrual cups and discs are listed in the FDA’s Unique Device Identification (UDI) database. This registry is required for Class II medical devices in the U.S., ensuring traceability and compliance with regulatory requirements.
How are the company’s devices classified under U.S. regulations?
The company’s menstrual cups and discs fall under Class II medical device classification in the U.S. This classification applies to devices with moderate risk, requiring special controls beyond general controls to ensure safety and effectiveness. The FDA’s UDI system tracks these devices to maintain regulatory oversight.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 840535440
Catalogue (20)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| AneerCare | A11 | FDA UDI | Class II | Active |
| AneerCare | B01 | FDA UDI | Class II | Active |
| AneerCare | A02 | FDA UDI | Class II | Active |
| AneerCare | V01 | FDA UDI | Class II | Active |
| AneerCare | A335 | FDA UDI | Class II | Active |
| AneerCare | A21 | FDA UDI | Class II | Active |
| AneerCare | Aneer | FDA UDI | Class II | Active |
| AneerCare | 337 | FDA UDI | Class II | Active |
| AneerCare | A99 | FDA UDI | Class II | Active |
| AneerCare | A18 | FDA UDI | Class II | Active |
| bassrose | 071 | FDA UDI | Class II | Active |
| AneerCare | A08 | FDA UDI | Class II | Active |
| AneerCare | A345 | FDA UDI | Class II | Active |
| AneerCare | A09 | FDA UDI | Class II | Active |
| AneerCare | A28 | FDA UDI | Class II | Active |
| AneerCare | A06 | FDA UDI | Class II | Active |
| AneerCare | 338 | FDA UDI | Class II | Active |
| AneerCare | A03 | FDA UDI | Class II | Active |
| AneerCare | A01 | FDA UDI | Class II | Active |
| AneerCare | A346 | FDA UDI | Class II | Active |
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