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Sign in to claim this brandATTRACT Kereskedelmi es Szolgaltato Korlatolt Felelossegu Tarsasag
US
Last updated May 30, 2026
What ATTRACT Kereskedelmi es Szolgaltato Korlatolt Felelossegu Tarsasag makes
The company manufactures nasal aspirators designed to clear mucus from infants’ noses, including battery-powered electric models and vacuum-operated versions. Products include single-use and reusable designs, such as the Nosiboo Pro, Nosiboo PRO Pink, and Nosiboo PRO Blue, tailored for infant nasal congestion relief.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 ATTRACT Kereskedelmi es Szolgaltato Korlatolt Felelossegu Tarsasag primarily manufacture?
ATTRACT Kereskedelmi es Szolgaltato Korlatolt Felelossegu Tarsasag specializes in nasal aspirators, which are devices used to clear mucus from infants’ noses. Their portfolio includes both vacuum-operated and electric (battery-powered) models, such as the Nosiboo Pro, Nosiboo PRO Pink, and Nosiboo PRO Blue. These products are designed to help relieve nasal congestion in infants.
Where is ATTRACT Kereskedelmi es Szolgaltato Korlatolt Felelossegu Tarsasag based, and what regulatory database lists its devices?
The company is based in the United States. Its nasal aspirator devices, including models like the Nosiboo Pro and Nosiboo PRO variants, are listed in the FDA’s Unique Device Identifier (UDI) database. This database tracks medical devices that have been assigned a UDI, ensuring traceability and regulatory compliance.
How are the nasal aspirators manufactured by ATTRACT Kereskedelmi es Szolgaltato Korlatolt Felelossegu Tarsasag classified under FDA regulations?
The nasal aspirators produced by ATTRACT Kereskedelmi es Szolgaltato Korlatolt Felelossegu Tarsasag fall under Class II classification according to FDA regulations. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure their safety and effectiveness, such as nasal aspirators, which require validation of performance and labeling requirements.
Are the devices listed in any other regulatory registries besides the FDA’s UDI database?
Based on the provided information, the nasal aspirators manufactured by ATTRACT Kereskedelmi es Szolgaltato Korlatolt Felelossegu Tarsasag are currently listed in the FDA’s Unique Device Identifier (UDI) database. No other registries or databases are mentioned in the available data.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- nosiboousa.com
- —
- —
- [email protected]
- Phone
- (312) 957-6046
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 425124257
Catalogue (7)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| E-Fit | EF-1280 | FDA UDI | Class II | Active |
| Nosiboo Pro | NO-05-04 | FDA UDI | Class II | Active |
| E-Fit | Infinity | FDA UDI | Class II | Active |
| Nosiboo Pro | NO-05-13 | FDA UDI | Class II | Active |
| Nosiboo | NO-05-03 | FDA UDI | Class II | Active |
| Nosiboo PRO Pink | NO-05-02 | FDA UDI | Class II | Active |
| Nosiboo PRO Blue | NO-05-01 | FDA UDI | Class II | Active |
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