Skip to content

Medline Industries, Inc. OR926K

by Medline Industries, Inc.

Ref OR926K

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

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

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0888277DC265NSKX Basic UDI-DI 40888277276223UDI-DIDate15 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number40888277276223 UDI-DI Date28 Aug 2018ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Medline Industries, Inc.
Generic Name
General surgical procedure kit, non-medicated, single-use
Device Name
Suction canister
Model / Ref / Catalog
OR926K
Primary DI / UDI-DI
40888277276223 EUDAMED
10888277276222 GUDID
Basic UDI-DI
0888277DC265NSKX
Unit of Use DI
10888277276222
FDA Product Code
JOL
EMDN Code
A06030401 Intraoperative suction containers
GMDN Term
General surgical procedure kit, non-medicated, single-use
Device Class
Class I EUDAMED
Class II GUDID
Regulation Number
880.6740
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
40888277276223
GUDID
10888277276222
Device ClassEUDAMED
Class I
GUDID
Class II

Related devices

Category: General surgical procedure kit, non-medicated, single-use

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Single Use
  • CMR Substance
  • Endocrine Disruptor
  • Prescription Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (16)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No