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Henry Schein 5701884

by Henry Schein, Inc.

Henry Schein 5701884 is an ear canal irrigation kit (FDA Class I; FDA product code KCP, Syringe, Ent) made by Henry Schein, Inc., listed in FDA GUDID since 28 Apr 2021 (UDI-DI 10304040127855), 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 Number10304040127855 UDI-DI Date28 Apr 2021ListedStatusListed 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  • Withdrawn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
Ear canal irrigation kit, reusable
Model / Ref / Catalog
5701884
Primary DI / UDI-DI
10304040127855
FDA product code
KCP
GMDN term
Ear canal irrigation kit, reusable
Device class
Class I
Regulation number
874.5220
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ear canal irrigation kit, reusable

Similar devices

Other devices filed under FDA product code KCP (SYRINGE, ENT).

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

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