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Henry Schein 5701316

by Henry Schein, Inc.

Henry Schein 5701316 is a Class I device made by Henry Schein, Inc., listed in FDA GUDID since 11 Jan 2019 (UDI-DI 10304040103866), 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 Number10304040103866 UDI-DI Date11 Jan 2019ListedStatusListed 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  • Withdrawn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
Medical equipment drape, single-use, non-sterile
Model / Ref / Catalog
5701316
Primary DI / UDI-DI
10304040103866
FDA product code
NRU
GMDN term
Medical equipment drape, single-use, non-sterile
Device class
Class I
Regulation number
872.6250
GUDID distribution status
In Commercial Distribution

Related devices

Category: Medical equipment drape, single-use, non-sterile

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)