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Sign in to claim this brandNingbo Albert Novosino Co., Ltd.
US
Last updated September 17, 2026
Part of Ningbo Albert Novosino Co., Ltd.
What Ningbo Albert Novosino Co., Ltd. makes
The company manufactures reusable intravenous pressure infusors for controlled fluid delivery, reusable earplugs for noise reduction, and single-use gravity enema sets for gastrointestinal procedures. It also produces blood pressure cuffs designed for one-time clinical use.
These devices are classified under FDA’s Class I and Class II regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. 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 Ningbo Albert Novosino Co., Ltd. manufacture?
Ningbo Albert Novosino Co., Ltd. produces a range of medical devices including reusable intravenous pressure infusors for controlled fluid delivery, reusable earplugs for noise reduction, single-use gravity enema sets for gastrointestinal procedures, and single-use blood pressure cuffs. These devices serve clinical needs across fluid therapy, patient comfort, and diagnostic monitoring.
Where is Ningbo Albert Novosino Co., Ltd. based?
The company operates from the United States. While its name suggests a Chinese origin, its manufacturing and regulatory activities are conducted within the US market.
Which regulatory registries list devices manufactured by Ningbo Albert Novosino Co., Ltd.?
Devices from Ningbo Albert Novosino Co., Ltd. are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers and regulators, allowing them to verify device details like model, batch, and manufacturer information.
How are devices from Ningbo Albert Novosino Co., Ltd. classified under FDA regulations?
The company’s devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher risk and may require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use and potential health impact.
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
- 543014978
Catalogue (18)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Biegler | JR5001000 | FDA UDI | Class I | Active |
| Biegler | JR6001000 | FDA UDI | Class I | Active |
| Premium | 2L | FDA UDI | Class I | Active |
| Biegler | JR5050201 | FDA UDI | Class I | Active |
| Biegler | JR6060201 | FDA UDI | Class I | Active |
| Clariflo | RU3000PGS | FDA UDI | Class I | Active |
| Clariflo | 500PGS | FDA UDI | Class I | Active |
| Clariflo | 3000PGS | FDA UDI | Class I | Active |
| Biegler | JR6060301 | FDA UDI | Class I | Active |
| Premium | 2L | FDA UDI | Class I | Active |
| Biegler | JR5050301 | FDA UDI | Class I | Active |
| Biegler | JR5003000 | FDA UDI | Class I | Active |
| Biegler | JR5000500 | FDA UDI | Class I | Active |
| Migraine stopper | 1.0 | FDA UDI | Class I | Active |
| Claricuff™ | Tapmedic | FDA UDI | Class II | Active |
| Biegler | JR6003000 | FDA UDI | Class I | Active |
| Migraine Stopper | A/0 | FDA UDI | Class I | Active |
| Clariflo | RU1000PGS | FDA UDI | Class I | Active |
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