Primary Device ID | 00815849023505 |
NIH Device Record Key | fe2e1b69-c50c-4890-9f58-336cabf3d55a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MPM |
Version Model Number | MPM-295 |
Company DUNS | 948904735 |
Company Name | CUSTOM ASSEMBLIES, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815849023505 [Primary] |
LRO | General Surgery Tray |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-09-21 |
Device Publish Date | 2023-09-13 |
00815849025059 | Procedure Kit |
00815849025042 | Procedure Kit |
00815849025035 | Procedure Kit |
00815849025028 | Procedure Kit |
00815849025004 | Procedure Kit |
00815849024946 | Procedure Kit |
00815849024939 | Procedure Kit |
00815849024922 | Procedure Kit |
00815849024649 | Procedure Kit |
00815849024465 | Procedure Kit |
00815849024359 | Procedure Kit |
00815849024212 | Procedure Kit |
00815849024199 | Procedure Kit |
00815849023819 | Procedure Kit |
00815849023505 | Procedure Kit |
00815849023482 | Procedure Kit |