Identification Labels 197823

GUDID 10886333208958

MLK Identification Labels with Marker

ARGON MEDICAL DEVICES, INC.

Procedural medication labelling set
Primary Device ID10886333208958
NIH Device Record Key5eb6ade9-f4a4-4265-91c1-2613825160fd
Commercial Distribution StatusIn Commercial Distribution
Brand NameIdentification Labels
Version Model Number197823
Catalog Number197823
Company DUNS140727624
Company NameARGON MEDICAL DEVICES, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100886333208951 [Primary]
GS110886333208958 [Package]
Contains: 00886333208951
Package: Box [5 Units]
In Commercial Distribution
GS120886333208955 [Package]
Package: Box [50 Units]
In Commercial Distribution

FDA Product Code

LYNApparatus, Visual Reinforcement Audiometric

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-07-29
Device Publish Date2022-07-21

Devices Manufactured by ARGON MEDICAL DEVICES, INC.

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