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Lma Atomization IPN048832

by Teleflex Incorporated

Lma Atomization IPN048832 (MAD515) is an atomizer (FDA Class I; FDA product code CCQ, Nebulizer, Medicinal, Non-Ventilatory (Atomizer)) made by Teleflex Incorporated, listed in FDA GUDID since 15 Sep 2018 (UDI-DI 14026704613165), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number14026704613165 UDI-DI Date15 Sep 2018ListedStatusListed 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  • Withdrawn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
Lma Atomization
Generic name
Atomizer, non-ventilatory
Model / Ref / Catalog
IPN048832, MAD515
Primary DI / UDI-DI
14026704613165
FDA product code
CCQ
GMDN term
Atomizer, non-ventilatory
Device class
Class I
Regulation number
868.5640
GUDID distribution status
In Commercial Distribution

Related devices

Category: Atomizer, non-ventilatory

Similar devices

Other devices filed under FDA product code CCQ (NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)).

Other devices from Teleflex Incorporated

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    Class II

  • Arrow IPNB00822 Open recall

    Class II

  • Arrow IPNB00827 Open recall

    Class II

See all devices from Teleflex Incorporated →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)