UDI device identifier

Moldex Airwave Surgical N95 Respirator 4150

UDI device identifier 00092311415000 · MOLDEX-METRIC, INC.

Key facts

Primary DI 00092311415000
Brand name Moldex Airwave Surgical N95 Respirator
Version or model 4150
Company MOLDEX-METRIC, INC.
DUNS number 066237736
Product code MSH
GMDN term Surgical/medical respirator, non-antimicrobial, single-use
Device class Class II
Single use Yes
Packaged sterile No
Implantable No
Publish date Feb 25, 2022
Version date Sep 13, 2023

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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