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Henry Schein 5700822

by Henry Schein, Inc.

Henry Schein 5700822 is a Class I device made by Henry Schein, Inc., listed in FDA GUDID since 24 Feb 2020 (UDI-DI 10304040065805), 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 Number10304040065805 UDI-DI Date24 Feb 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  • Withdrawn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
Henry Schein
Generic name
Endoscopic bite block, basic, single-use
Model / Ref / Catalog
5700822
Primary DI / UDI-DI
10304040065805
FDA product code
EGZ
GMDN term
Endoscopic bite block, basic, single-use
Device class
Class I
Regulation number
872.1905
GUDID distribution status
In Commercial Distribution
Sterilisation method
Liquid Chemical

Related devices

Category: Endoscopic bite block, basic, single-use

Similar devices in this category

Other devices filed under Endoscopic bite block, basic, single-use.

Other devices from Henry Schein, Inc.

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Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)