UDI device identifier

Vermed 20300-18-RED

UDI device identifier 00009336008223 · GRAPHIC CONTROLS ACQUISITION CORP

Key facts

Primary DI 00009336008223
Brand name Vermed
Version or model 20300-18-RED
Catalog number 20300-18-RED
Company GRAPHIC CONTROLS ACQUISITION CORP
DUNS number 002111896
Product code DSA
GMDN term Electrocardiographic lead set, reusable
Premarket submission K942321
Device class Class II
Single use No
Packaged sterile No
Implantable No
Publish date Feb 28, 2017
Version date Jul 27, 2026
Description Din Lead Wire .080, Snap to Socket, 18", Red

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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