UDI device identifier

EM L815000A

UDI device identifier 00026072025987 · Allied Medical, LLC

Key facts

Primary DI 00026072025987
Brand name EM
Version or model L815000A
Company Allied Medical, LLC
DUNS number 119066872
Product code FMR
GMDN term Spine board
Device class Class I
Single use No
Packaged sterile No
Implantable No
Publish date May 28, 2024
Version date Oct 13, 2025
Description XTRA BACKBOARD,RED,NO PINS

At a glance

  • None MAUDE reports citing this UDI
  • No Linked premarket submission
  • No EUDAMED counterpart found
  • 100–999 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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