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Henry Schein 900-7487

by Henry Schein, Inc.

Henry Schein 900-7487 is a Class II device made by Henry Schein, Inc., listed in FDA GUDID since 25 Sep 2015 (UDI-DI 00304040000168), 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 Number00304040000168 UDI-DI Date25 Sep 2015ListedStatusListed 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  • Withdrawn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
Nylon suture, non-bioabsorbable, monofilament
Model / Ref / Catalog
900-7487
Primary DI / UDI-DI
00304040000168
FDA product code
GAR
GMDN term
Nylon suture, non-bioabsorbable, monofilament
Device class
Class II
Regulation number
878.5020
GUDID distribution status
In Commercial Distribution

Related devices

Category: Nylon suture, non-bioabsorbable, monofilament

Similar devices in this category

Other devices filed under Nylon suture, non-bioabsorbable, monofilament.

Other devices from Henry Schein, Inc.

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)