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CLEARinse

FDA UDI

Class II (US FDA UDI)

by Peno Llc

Identity

Trade Name
CLEARinse FDA UDI
Generic Name
Nasal aspirator, electric FDA UDI
Device Name
The CLEARinse Pro is designed to make nasal and sinus lavage easy and convenient. The device facilitates instillation of saline into the nasal passage. It then provides mild powered suction to remove the fluid from the nostril. Alternatively, it can be used on the opposite nostril while intermittently occluding the sprayed nostril, i.e., the Proetz Displacement maneuver. The device consists of a hand held battery operated unit with a disposable tip portion. A charger is provided with the device. FDA UDI
Model / Reference
Pro FDA UDI
Description
The CLEARinse Pro is designed to make nasal and sinus lavage easy and convenient. The device facilitates instillation of saline into the nasal passage. It then provides mild powered suction to remove the fluid from the nostril. Alternatively, it can be used on the opposite nostril while intermittently occluding the sprayed nostril, i.e., the Proetz Displacement maneuver. The device consists of a hand held battery operated unit with a disposable tip portion. A charger is provided with the device. FDA UDI

Identifiers

Primary DI / UDI-DI
B423CRPRO1 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nasal aspirator, electric

CLEARinse by Peno Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal aspirator, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Peno Llc

Sources (1)

  • FDA UDI 437344d1-2b80-44f7-a633-5df29c17f847 34 fields · synced Jun 8, 2026