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Centurion® 8065752527

by Alcon Laboratories, Inc.

Centurion® 8065752527 is a Class II device made by Alcon Laboratories, Inc., listed in FDA GUDID since 31 Aug 2020 (UDI-DI 00380657525270), 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 Number00380657525270 UDI-DI Date31 Aug 2020ListedStatusListed 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  • Withdrawn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
Centurion®
Generic name
Medical device integration rack
Model / reference
8065752527
Primary DI / UDI-DI
00380657525270
FDA product code
HQC
GMDN term
Medical device integration rack
Device class
Class II
Regulation number
886.4670
GUDID distribution status
In Commercial Distribution

Related devices

Category: Medical device integration rack

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Other devices filed under Medical device integration rack.

Other devices from Alcon Laboratories, Inc.

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Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)