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superDimension AED00170-01

by Covidien LP

superDimension AED00170-01 is a Class II device made by Covidien LP, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10884521582835), 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 Number10884521582835 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
superDimension
Generic name
Portable computer
Model / reference
AED00170-01
Primary DI / UDI-DI
10884521582835
FDA product code
JAK
GMDN term
Portable computer
Device class
Class II
Regulation number
892.1750
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code JAK (System, x-ray, tomography, computed).

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See all devices from Covidien LP →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)