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Steri-Shield 088-022

by Steri-Shield Products, Inc.

Steri-Shield 088-022 is a Class I device made by Steri-Shield Products, Inc., listed in FDA GUDID since 3 Jun 2022 (UDI-DI 10850040097013), 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 Number10850040097013 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  • Withdrawn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
Medical equipment/instrument drape, single-use
Model / reference
088-022
Primary DI / UDI-DI
10850040097013
FDA product code
EIA
GMDN term
Medical equipment/instrument drape, single-use
Device class
Class I
Regulation number
872.6640
GUDID distribution status
In Commercial Distribution

Related devices

Category: Medical equipment/instrument drape, single-use

Similar devices in this category

Other devices filed under Medical equipment/instrument drape, single-use.

Other devices from Steri-Shield Products, Inc.

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Properties

  • Single use
  • Contains latex
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)