Identity
- Trade Name
- CVS Health FDA UDI
- Generic Name
- Nasal aspirator, electric FDA UDI
- Device Name
- A portable, hand-held, battery powered suction device designed to enable an adult to gently suction and clear excessive mucus from the nasal passages of an infant or child to facilitate easier breathing. It consists of a hand grip that contains the batteries, a small electric pump that creates the suction, and a silicone nozzle attached to a detachable, washable, collection cup at the distal end. It is designed for domestic use and is applied superficially the nasal opening (i.e., not inserted into the nasal cavity). This is a reusable device. FDA UDI
- Model / Reference
- NS18 FDA UDI
- Description
- A portable, hand-held, battery powered suction device designed to enable an adult to gently suction and clear excessive mucus from the nasal passages of an infant or child to facilitate easier breathing. It consists of a hand grip that contains the batteries, a small electric pump that creates the suction, and a silicone nozzle attached to a detachable, washable, collection cup at the distal end. It is designed for domestic use and is applied superficially the nasal opening (i.e., not inserted into the nasal cavity). This is a reusable device. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00050428550014 FDA UDI
- FDA Product Code
- JCX FDA UDI
- GMDN Term
- Nasal aspirator, electric FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4780 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Nasal aspirator, electric
CVS Health by Woonsocket Prescription Center, Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Woonsocket Prescription Center, Incorporated
Sources (1)
- FDA UDI 4c4b34d3-e7b7-401d-969c-a5841094ec75 34 fields · synced Jun 1, 2026