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Fridababy

FDA UDI

Class II (US FDA UDI)

by Fridababy, LLC

Identity

Trade Name
Fridababy FDA UDI
Generic Name
Nasal aspirator, electric FDA UDI
Device Name
Electric Nasal Aspirator Model 12300100 FDA UDI
Model / Reference
12300100 FDA UDI
Description
Electric Nasal Aspirator Model 12300100 FDA UDI

Identifiers

Primary DI / UDI-DI
00810028776739 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Nasal aspirator, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

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

Fridababy by Fridababy, 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
Fridababy, LLC

Sources (1)

  • FDA UDI 54796333-7e54-4e0b-8f10-3689e29d72a1 34 fields · synced Jun 6, 2026