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Fridababy 12300100

by Fridababy, LLC

Fridababy 12300100 is a Class II device made by Fridababy, LLC, listed in FDA GUDID since 8 Jan 2025 (UDI-DI 00810028776739), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810028776739 UDI-DI Date8 Jan 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Fridababy
Generic name
Nasal aspirator, electric
Model / reference
12300100
Primary DI / UDI-DI
00810028776739
FDA product code
KDQ
GMDN term
Nasal aspirator, electric
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KDQ (Bottle, Collection, Vacuum).

Other devices from Fridababy, LLC

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Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)