UDI device identifier

MEDLINE ART535A

UDI device identifier 10653160367604 · MEDLINE INDUSTRIES, INC.

Key facts

Primary DI 10653160367604
Brand name MEDLINE
Version or model ART535A
Catalog number ART535A
Company MEDLINE INDUSTRIES, INC.
DUNS number 025460908
Product code LRO
GMDN term General surgical procedure kit, medicated
Premarket submission K213481
Device class Class II
Single use Yes
Packaged sterile Yes
Implantable No
Publish date Oct 23, 2023
Version date Oct 31, 2023
Description ARTERIAL LINE BUNDLE - OR

At a glance

  • None MAUDE reports citing this UDI
  • Yes Linked premarket submission
  • No EUDAMED counterpart found
  • 1,000+ GUDID devices with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About UDI device identifiers (GUDID)

The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.

Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date:

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