Sage Lateral Transfer Mat

GUDID 10816317023475

Prevalon AirTAP Glide Sheet

RENU MEDICAL, INC

Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat Patient transfer sliding mat
Primary Device ID10816317023475
NIH Device Record Keyec91aad9-f686-4014-9c69-5a2b7d446f1c
Commercial Distribution StatusIn Commercial Distribution
Brand NameSage Lateral Transfer Mat
Version Model NumberRM-7219
Company DUNS100439103
Company NameRENU 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 Usetrue
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100816317023478 [Primary]
GS110816317023475 [Package]
Contains: 00816317023478
Package: Case [10 Units]
In Commercial Distribution

FDA Product Code

FMRDevice, Transfer, Patient, Manual

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-07-07
Device Publish Date2023-06-29

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