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Sign in to claim this brandCARDICARE COMPANY LTD
US
Last updated May 30, 2026
What CARDICARE COMPANY LTD makes
Cardicare Company Ltd manufactures aneroid manual sphygmomanometers, including single-use models and those integrated with stethoscopes. These devices are designed for measuring blood pressure in clinical and home settings, featuring mechanical cuff inflation and mercury-free mercury column technology.
The company’s products fall under FDA Class II regulation, with devices listed under 510(k) clearance and included in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in 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 Cardicare Company Ltd manufacture?
Cardicare Company Ltd specializes in aneroid manual sphygmomanometers, which are blood pressure measurement devices. These include standard models and single-use variants, as well as cuffs integrated with stethoscopes. Their products rely on mechanical cuff inflation and mercury-free mercury column technology, suitable for both clinical and home use.
Where is Cardicare Company Ltd based?
Cardicare Company Ltd is headquartered in the United States. The company’s location influences its regulatory compliance, particularly with U.S. authorities like the FDA.
Which regulatory registries list Cardicare Company Ltd’s devices?
Cardicare Company Ltd’s devices are listed in the FDA’s 510(k) clearance registry and the FDA’s Unique Device Identifier (UDI) database. These registries track devices that have undergone premarket notification (510(k)) and are assigned a UDI for traceability and compliance.
How are Cardicare Company Ltd’s devices classified by regulatory authorities?
Cardicare Company Ltd’s aneroid manual sphygmomanometers fall under FDA Class II classification. This classification applies to devices that pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- cardicare.net
- —
- —
- [email protected]
- Phone
- 13758279955
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 528101293
Catalogue (9)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| ASA Techmed | AS-MC | FDA UDI | Class II | Active |
| GRX Medical | BP-02 | FDA UDI | Class II | Unknown |
| ASA Techmed | AS-MC-PED | FDA UDI | Class II | Active |
| ASA Techmed | AS-MC-TH | FDA UDI | Class II | Active |
| GRX Medical | BP-01 | FDA UDI | Class II | Unknown |
| ASA Techmed | AS-MC-OB | FDA UDI | Class II | Active |
| ASA Techmed | AS-MC+SR KIT | FDA UDI | Class II | Active |
| Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer | K222652 | FDA 510(k) | Class II | Active |
| Aneroid Sphygmomanometer With Stethoscope Model Hbpk-A | K082542 | FDA 510(k) | Class II | Active |
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