Primary Device ID | 00815212021268 |
NIH Device Record Key | 5c11b749-0a46-47c0-8fbf-0abfa03650e0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vacuum Bag |
Version Model Number | VB2550225B |
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 | false |
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 | 00815212021268 [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 | 2016-12-13 |
00815212023002 | VB1508055 |
00815212021329 | VB1045320NV |
00815212021312 | VB1007030NV |
00815212021305 | VB707020B |
00815212021299 | VB707020 |
00815212021282 | VB507015B |
00815212021275 | VB507015 |
00815212021268 | VB2550225B |
00815212021251 | VB2550225 |
00815212021244 | VB20251B |
00815212021237 | VB20251 |
00815212021220 | VB200100120B |
00815212021213 | VB200100120 |
00815212021206 | VB1507560B |
00815212021190 | VB1507560 |
00815212021183 | VB15010075B |
00815212021176 | VB15010075 |
00815212021169 | VB1045320 |
00815212021152 | VB1007040B |
00815212021145 | VB1007040 |
00815212021138 | VB1007035B |
00815212021121 | VB1007035 |
00815212021114 | VB1007030B |
00815212021107 | VB1007030 |
00815212021091 | VB1006021 |
00815212021084 | VB10010040B |
00815212021077 | VB10010040 |