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Enova Illumination 80800-003

by Enova Illumination, Inc

Enova Illumination 80800-003 is a Class I device made by Enova Illumination, Inc, listed in FDA GUDID since 27 Jan 2022 (UDI-DI 00850025993340), 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 Number00850025993340 UDI-DI Date27 Jan 2022ListedStatusListed 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  • Withdrawn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
Enova Illumination
Generic name
Electrical-only medical device connection cable, reusable
Model / reference
80800-003
Primary DI / UDI-DI
00850025993340
FDA product code
HPP
GMDN term
Electrical-only medical device connection cable, reusable
Device class
Class I
Regulation number
886.4335
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrical-only medical device connection cable, reusable

Other devices from Enova Illumination, Inc

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Properties

  • Premarket exempt
Other properties (14, all answered No)