Primary Device ID | 30857182006013 |
NIH Device Record Key | fbcbfa34-ccfd-431e-8c17-3ce353fed239 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ULTRAGLIDE |
Version Model Number | 283 |
Company DUNS | 792740578 |
Company Name | INNOVATIVE MEDICAL TECHNOLOGIES, INC |
Device Count | 50 |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Needle Gauge | 23 Gauge |
Needle Gauge | 23 Gauge |
Needle Gauge | 23 Gauge |
Needle Gauge | 23 Gauge |
Needle Gauge | 23 Gauge |
Needle Gauge | 23 Gauge |
Needle Gauge | 23 Gauge |
Needle Gauge | 23 Gauge |
Needle Gauge | 23 Gauge |
Needle Gauge | 23 Gauge |
Needle Gauge | 23 Gauge |
Needle Gauge | 23 Gauge |
Needle Gauge | 23 Gauge |
Needle Gauge | 23 Gauge |
Needle Gauge | 23 Gauge |
Needle Gauge | 23 Gauge |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00857182006159 [Unit of Use] |
GS1 | 30857182006013 [Package] Contains: 40857182006010 Package: CS [20 Units] In Commercial Distribution |
GS1 | 40857182006010 [Primary] |
FMI | Needle, Hypodermic, Single Lumen |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2018-05-09 |
30857182006020 | SAFETY BLOOD COLLECTION SET 25G |
30857182006013 | SAFETY BLOOD COLLECTION SET 23G |
30857182006006 | SAFETY BLOOD COLLECTION SET 21G |