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Henry Schein 5700410

by Henry Schein, Inc.

Henry Schein 5700410 is a Class II device made by Henry Schein, Inc., listed in FDA GUDID since 21 May 2018 (UDI-DI 00304040029176), 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 Number00304040029176 UDI-DI Date21 May 2018ListedStatusListed 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  • Withdrawn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
Dental anaesthesia syringe, reusable
Model / Ref / Catalog
5700410
Primary DI / UDI-DI
00304040029176
FDA product code
EJI
GMDN term
Dental anaesthesia syringe, reusable
Device class
Class II
Regulation number
872.6770
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 5.5 Inch

Related devices

Category: Dental anaesthesia syringe, reusable

Similar devices

Other devices filed under FDA product code EJI (Syringe, cartridge).

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

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