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Powervision Imaging System 102

by Corindus, Inc.

Powervision Imaging System 102 is a Class I device made by Corindus, Inc., listed in FDA GUDID since 25 Jan 2017 (UDI-DI 00816280021020), not in commercial distribution (GUDID) as of 22 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number00816280021020 UDI-DI Date25 Jan 2017ListedStatusListed GUDID: not 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  • Withdrawn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
Powervision Imaging System
Generic name
Image display unit, colour
Model / Ref / Catalog
102
Primary DI / UDI-DI
00816280021020
FDA product code
OUG
GMDN term
Image display unit, colour
Device class
Class I
Regulation number
880.6310
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code OUG (Medical Device Data System).

Other devices from Corindus, Inc.

See all devices from Corindus, Inc. →

Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)