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Steri-Shield 088-052

by Steri-Shield Products, Inc.

Steri-Shield 088-052 is a Class I device made by Steri-Shield Products, Inc., listed in FDA GUDID since 3 Jun 2022 (UDI-DI 10850040097266), 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 Number10850040097266 UDI-DI Date3 Jun 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  • Withdrawn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
Steri-Shield
Generic name
Dental x-ray film holder, single-use
Model / reference
088-052
Primary DI / UDI-DI
10850040097266
FDA product code
EGZ
GMDN term
Dental x-ray film holder, single-use
Device class
Class I
Regulation number
872.1905
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental x-ray film holder, single-use

Similar devices

Other devices filed under FDA product code EGZ (Holder, Film, X-Ray).

Other devices from Steri-Shield Products, Inc.

See all devices from Steri-Shield Products, Inc. →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)