UDI device identifier

CVS MD300CN330R

UDI device identifier 00050428167335 · WOONSOCKET PRESCRIPTION CENTER, INCORPORATED

Key facts

Primary DI 00050428167335
Brand name CVS
Version or model MD300CN330R
Company WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
DUNS number 062312574
Product code PGJ
GMDN term Pulse oximeter
Device class Class II
Single use No
Packaged sterile No
Implantable No
Publish date Jul 10, 2026
Version date Jul 20, 2026
Description CVS RESP RATE PULSE OXIMETER

At a glance

  • None MAUDE reports citing this UDI
  • No Linked premarket submission
  • No EUDAMED counterpart found
  • 10–99 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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