DRY320

GUDID 00860010835234

A device to store and dry endoscopes

Wassenburg Medical, Inc.

Endoscope drying/storage cabinet
Primary Device ID00860010835234
NIH Device Record Key9fadbdf8-48ab-46aa-8e52-02c265985091
Commercial Distribution StatusIn Commercial Distribution
Brand NameDRY320
Version Model NumberDRY320
Company DUNS118762097
Company NameWassenburg Medical, 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 Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone12153641477
Emailm.infanti@wassenburgmedical.com
Phone12153641477
Emailm.infanti@wassenburgmedical.com
Phone12153641477
Emailm.infanti@wassenburgmedical.com
Phone12153641477
Emailm.infanti@wassenburgmedical.com
Phone12153641477
Emailm.infanti@wassenburgmedical.com
Phone12153641477
Emailm.infanti@wassenburgmedical.com
Phone12153641477
Emailm.infanti@wassenburgmedical.com
Phone12153641477
Emailm.infanti@wassenburgmedical.com
Phone12153641477
Emailm.infanti@wassenburgmedical.com
Phone12153641477
Emailm.infanti@wassenburgmedical.com
Phone12153641477
Emailm.infanti@wassenburgmedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100860010835234 [Primary]

FDA Product Code

JRJUnit, Drying

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-05-01
Device Publish Date2024-04-23

On-Brand Devices [DRY320]

G434DRY320A device to store and dry endoscopes
00860010835234A device to store and dry endoscopes

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.