Primary Device ID | 00815212020506 |
NIH Device Record Key | 8de83ecc-827c-4446-b1c2-d67222c7bcab |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Quick Spherz |
Version Model Number | QS7004 |
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 | 00815212020506 [Primary] |
HAW | Neurological Stereotaxic Instrument |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-11-03 |
00815212021657 | 2021-40 |
00815212021640 | 2021-160 |
00815212021633 | 2021-130 |
00815212021626 | 2021-120 |
00815212021619 | 2021-100 |
00815212021602 | 2021-04 |
00815212021596 | 2021-03 |
00815212021572 | 2021-01 |
00815212020520 | QS7090 |
00815212020513 | QS7005 |
00815212020506 | QS7004 |
00815212020490 | QS7003 |
00815212020483 | QS7002 |
00815212020476 | QS7001 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
QUICK SPHERZ 86025808 4625939 Live/Registered |
IZI Medical Products, LLC 2013-08-01 |
QUICK SPHERZ 86025779 4625937 Live/Registered |
IZI Medical Products, LLC 2013-08-01 |