McKessan

GUDID 00612479258181

Pressure Prevention Group 1 Surfaces Product Description APP Sys,Dlx,Variable Pressure,1/ea

Drive Devilbiss Healthcare

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Primary Device ID00612479258181
NIH Device Record Keya39e4e81-c0d0-4d64-8582-f25557b85c0e
Commercial Distribution StatusIn Commercial Distribution
Brand NameMcKessan
Version Model Number146-14001E
Company DUNS867673159
Company NameDrive Devilbiss Healthcare
Device Count1
DM Exempttrue
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS100612479258181 [Primary]

FDA Product Code

FNMMATTRESS, AIR FLOTATION, ALTERNATING PRESSURE

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-03-05
Device Publish Date2021-02-25

On-Brand Devices [McKessan]

00822383007489Pressure Prevention Group 2 Surfaces Product Description Med Aire Low Air Loss, 8in 1/cs
00612479258181Pressure Prevention Group 1 Surfaces Product Description APP Sys,Dlx,Variable Pressure,1/ea

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