UDI device identifier

2E7554

UDI device identifier 00085412563718 · BAXTER INTERNATIONAL INC.

Key facts

Primary DI 00085412563718
Version or model 2E7554
Catalog number 2E7554
Company BAXTER INTERNATIONAL INC.
DUNS number 005146311
Product code FPA
GMDN term Electric infusion pump administration set, single-use
Premarket submission K161323
Device class Class II
Single use Yes
Packaged sterile Yes
Implantable No
Publish date Feb 17, 2017
Version date Jul 6, 2018
Description Solution Set, Male Epidural Non-Luer Lock Adapter For Epidural Use

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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