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Henry Schein 5700620

by Henry Schein, Inc.

Henry Schein 5700620 is a Class I device made by Henry Schein, Inc., listed in FDA GUDID since 13 Jul 2017 (UDI-DI 00304040057100), 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 Number00304040057100 UDI-DI Date13 Jul 2017ListedStatusListed 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  • Withdrawn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
Skin staple remover, single-use
Model / Ref / Catalog
5700620
Primary DI / UDI-DI
00304040057100
FDA product code
HBS
GMDN term
Skin staple remover, single-use
Device class
Class I
Regulation number
882.4190
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide

Related devices

Category: Skin staple remover, single-use

Other devices from Henry Schein, Inc.

See all devices from Henry Schein, Inc. →

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Prescription use
  • Combination product
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)