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ClearNose Nasal Aspirator

FDA UDI

Class I (US FDA UDI)

by Munchkin Inc.

Identity

Trade Name
ClearNose Nasal Aspirator FDA UDI
Generic Name
Nasal aspirator, manual FDA UDI
Device Name
Relieves nasal congestion Designed to reduce the spreading of germs Three different sized nose tips and storage case FDA UDI
Model / Reference
10681 FDA UDI
Description
Relieves nasal congestion Designed to reduce the spreading of germs Three different sized nose tips and storage case FDA UDI

Identifiers

Primary DI / UDI-DI
00735282106811 FDA UDI
FDA Product Code
KYZ FDA UDI
GMDN Term
Nasal aspirator, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6960 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, manual

ClearNose Nasal Aspirator by Munchkin Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal aspirator, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Munchkin Inc.

Sources (1)

  • FDA UDI 721b2f07-78b2-4e16-9f2f-6cb077876a5d 34 fields · synced Jun 8, 2026