UDI device identifier

Halyard WAFB208-02_0002

UDI device identifier 10809160424759 · AVID MEDICAL, INC.

Key facts

Primary DI 10809160424759
Brand name Halyard
Version or model WAFB208-02_0002
Catalog number WAFB208-02
Company AVID MEDICAL, INC.
DUNS number 015623119
Product code OES
GMDN term Central venous catheterization kit, short-term
Device class Class II
Single use Yes
Packaged sterile Yes
Implantable No
Publish date May 3, 2024
Version date May 13, 2024

At a glance

  • None MAUDE reports citing this UDI
  • No 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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