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Sign in to claim this brandCarencease Healthcare LLC
US
Last updated May 24, 2026
What Carencease Healthcare LLC makes
Carencease Healthcare LLC manufactures first aid absorbent pads and bandages designed to control external bleeding, including the BleedCEASE® line, as well as nasal haemostatic plugs like NasalCEASE®. These products are intended for immediate use in wound management and nasal bleeding control. The company also produces variations of its BleedCEASE® product for specific applications.
The company’s portfolio consists of Class II (U) devices under FDA regulations, with all products listed in the FDA’s Unique Device Identifier (UDI) database. These devices are intended for use within the United States and comply with applicable U.S. medical device standards.
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 Carencease Healthcare LLC manufacture?
Carencease Healthcare LLC specializes in two primary categories of medical devices: first aid absorbent pads and bandages, such as the BleedCEASE® line, which are designed to control external bleeding; and nasal haemostatic plugs, like NasalCEASE®, intended for managing nasal bleeding. These products are focused on immediate wound management and are engineered for quick, effective use in emergency or first aid situations.
Where is Carencease Healthcare LLC based, and where are its devices intended for use?
Carencease Healthcare LLC is based in the United States. Its devices, including BleedCEASE® and NasalCEASE®, are specifically intended for use within the U.S. market, adhering to applicable U.S. medical device regulations and standards.
Which regulatory registries or databases list Carencease Healthcare LLC’s devices?
Carencease Healthcare LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency of medical devices under U.S. regulatory oversight, helping healthcare providers and authorities identify and verify the products.
How are Carencease Healthcare LLC’s devices classified under U.S. regulations?
Carencease Healthcare LLC’s devices fall under the classification of Class II (denoted as 'U') under FDA regulations. This classification is typically assigned to devices that pose moderate risk and require special controls in addition to general controls to ensure their safety and effectiveness, such as first aid and haemostatic products.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- catalina-healthcare.com
- —
- —
- [email protected]
- Phone
- 585-624-7540
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 080452143
Catalogue (4)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| BleedCEASE® | CAT BC-25 | FDA UDI | U | Active |
| BleedCEASE® | CAT BC-5 | FDA UDI | U | Active |
| NasalCEASE® | CAT NAS-5 | FDA UDI | U | Active |
| BleedCEASE® | CAT BC-100 | FDA UDI | U | Active |
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