UDI device identifier

Advance Plus Universal IV Administration Set 1720WY

UDI device identifier 00020221117202 · Exel International

Key facts

Primary DI 00020221117202
Brand name Advance Plus Universal IV Administration Set
Version or model 1720WY
Catalog number 1720WY
Company Exel International
DUNS number 180572216
Product code FPA
GMDN term Basic intravenous administration set, noninvasive
Premarket submission K092172
Device class Class II
Single use Yes
Packaged sterile Yes
Implantable No
Publish date Sep 26, 2016
Version date May 6, 2024
Description IV Administration Set, Luer Slip, 1 injection site, 20" tubing

At a glance

  • None MAUDE reports citing this UDI
  • Yes Linked premarket submission
  • Yes 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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