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Medline Industries, Inc. DYNJ905209B

by Medline Industries, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10193489347364 UDI-DI Date23 May 2021ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Medline Industries, Inc.
Generic Name
General surgical procedure kit, medicated
Model / Ref / Catalog
DYNJ905209B
Primary DI / UDI-DI
10193489347364
FDA Product Code
OEZ
GMDN Term
General surgical procedure kit, medicated
Device Class
Class II
Regulation Number
870.1200
GUDID distribution status
In Commercial Distribution

Related devices

Category: General surgical procedure kit, medicated

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Single Use
  • Contains Latex
  • Prescription Use
  • Convenience Kit
  • Combination Product
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (6)

  • Sterile: No
  • Implantable: No
  • Over-the-Counter: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No