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Henry Schein 5703105

by Henry Schein, Inc.

Henry Schein 5703105 is a Class I device made by Henry Schein, Inc., listed in FDA GUDID since 31 Jul 2023 (UDI-DI 10304040165154), 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 Number10304040165154 UDI-DI Date31 Jul 2023ListedStatusListed 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  • Withdrawn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
General-body orifice lubricant
Model / Ref / Catalog
5703105
Primary DI / UDI-DI
10304040165154
FDA product code
KMJ
GMDN term
General-body orifice lubricant
Device class
Class I
Regulation number
880.6375
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-body orifice lubricant

Similar devices

Other devices filed under FDA product code KMJ (Lubricant, patient).

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Expiration date
Other properties (8, all answered No)