Identity
- Trade Name
- CLEARinse Nasal Aspirator FDA UDI
- Generic Name
- Nasal aspirator, electric FDA UDI
- Model / Reference
- CR-BF FDA UDI
Identifiers
- Primary DI / UDI-DI
- CRBFV2 FDA UDI
- FDA Product Code
- KCJ FDA UDI
- GMDN Term
- Nasal aspirator, electric FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.5220 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
Yes
FDA UDI
Category: Nasal aspirator, electric
CLEARinse Nasal Aspirator by Peno Llc — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Peno Llc
Sources (1)
- FDA UDI ad8c1976-85a8-4f5d-ab2b-9c49b6bee5c8 33 fields · synced Jun 1, 2026