Safety Centesis Tray A30-CE3SFDF

GUDID 20886333220452

Safety Centesis Tray with Safety Devices and without Catheter and without Lidocaine

ARGON MEDICAL DEVICES, INC.

Aspiration tray, single-use
Primary Device ID20886333220452
NIH Device Record Key7467f702-5591-4713-92d3-56a9cf90fb6e
Commercial Distribution StatusIn Commercial Distribution
Brand NameSafety Centesis Tray
Version Model NumberA30-CE3SFDF
Catalog NumberA30-CE3SFDF
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 Kittrue
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
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100886333220458 [Primary]
GS120886333220452 [Package]
Contains: 00886333220458
Package: Box [10 Units]
In Commercial Distribution

FDA Product Code

OJTAspiration Tray

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-07-28
Device Publish Date2022-07-20

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