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Henry Schein 5700890

by Henry Schein, Inc.

Henry Schein 5700890 is a Class II device made by Henry Schein, Inc., listed in FDA GUDID since 30 Oct 2019 (UDI-DI 10304040071004), 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 Number10304040071004 UDI-DI Date30 Oct 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  • Withdrawn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
Electrosurgical system
Model / Ref / Catalog
5700890
Primary DI / UDI-DI
10304040071004
FDA product code
HGI
GMDN term
Electrosurgical system
Device class
Class II
Regulation number
884.4120
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrosurgical system

Similar devices in this category

Other devices filed under Electrosurgical system.

Other devices from Henry Schein, Inc.

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Properties

  • Single use
  • Prescription use
Other properties (13, all answered No)