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Aeroneb Module control cable 6687685

by Maquet Critical Care AB

Aeroneb Module control cable 6687685 is a Class II device made by Maquet Critical Care AB, listed in FDA GUDID since 23 Oct 2015 (UDI-DI 07325710002841), 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 Number07325710002841 UDI-DI Date23 Oct 2015ListedStatusListed 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  • Withdrawn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
Aeroneb Module control cable
Generic name
Neonatal/adult intensive-care ventilator
Model / reference
6687685
Primary DI / UDI-DI
07325710002841
FDA product code
CBK
GMDN term
Neonatal/adult intensive-care ventilator
Device class
Class II
Regulation number
868.5895
GUDID distribution status
In Commercial Distribution

Related devices

Category: Neonatal/adult intensive-care ventilator

Similar devices in this category

Other devices filed under Neonatal/adult intensive-care ventilator.

Other devices from Maquet Critical Care AB

See all devices from Maquet Critical Care AB →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)