Primary Device ID | 00815212020278 |
NIH Device Record Key | 3b522625-8395-40cf-bd61-9f33364f1e75 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Multi-Modality Markers |
Version Model Number | 52160 |
Company DUNS | 933506164 |
Company Name | Izi Medical Products, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
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 | 00815212020278 [Primary] |
IYE | Accelerator, Linear, Medical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-01-25 |
00815212022869 | S-MM3005 |
00815212022845 | S-MM3002 |
00815212022784 | MM3005-VIP |
00815212022777 | MM3005CLM |
00815212022753 | REG3002 |
00815212020773 | MM3007 |
00815212020766 | MM3005 |
00815212020759 | MM3003 |
00815212020742 | MM3002-60 |
00815212020735 | MM3002-10I |
00815212020728 | MM3002-100 |
00815212020711 | MM3002-10 |
00815212020704 | MM3002 |
00815212020278 | 52160 |
00815212020261 | 960-991 |
10815212020268 | 960-991 |