MPM

GUDID 00815849024922

Procedure Kit

CUSTOM ASSEMBLIES, INC.

General surgical procedure kit, non-medicated, single-use
Primary Device ID00815849024922
NIH Device Record Key06ff49bd-26fb-482b-9788-c8bb59772cee
Commercial Distribution StatusIn Commercial Distribution
Brand NameMPM
Version Model NumberMPM-318
Company DUNS948904735
Company NameCUSTOM ASSEMBLIES, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100815849024922 [Primary]

FDA Product Code

LROGeneral Surgery Tray

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-09-21
Device Publish Date2023-09-13

On-Brand Devices [MPM]

00815849025059Procedure Kit
00815849025042Procedure Kit
00815849025035Procedure Kit
00815849025028Procedure Kit
00815849025004Procedure Kit
00815849024946Procedure Kit
00815849024939Procedure Kit
00815849024922Procedure Kit
00815849024649Procedure Kit
00815849024465Procedure Kit
00815849024359Procedure Kit
00815849024212Procedure Kit
00815849024199Procedure Kit
00815849023819Procedure Kit
00815849023505Procedure Kit
00815849023482Procedure Kit

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