UDI device identifier

GoodSense 180410000880

UDI device identifier 00180410000880 · GEISS, DESTIN & DUNN, INC

Key facts

Primary DI 00180410000880
Brand name GoodSense
Version or model 180410000880
Company GEISS, DESTIN & DUNN, INC
DUNS number 076059836
Product code NAB
GMDN term Non-woven gauze pad
Device class Class I
Single use Yes
Packaged sterile Yes
Implantable No
Publish date Aug 28, 2020
Version date Nov 7, 2024
Description Sterile Pads, all one size, 3 IN x 3 IN (76 mm x 76 mm)

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:

Browse all UDI device identifiers (GUDID)