Primary Device ID | 10850048235004 |
NIH Device Record Key | f9dc4e6b-501d-42c7-9b8f-957897d61a03 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HMG |
Version Model Number | 001 |
Company DUNS | 117654675 |
Company Name | Hartman Medical Group LLC |
Device Count | 2000 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
Manufacturing Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850048235038 [Unit of Use] |
GS1 | 10850048235004 [Primary] |
DRX | Electrode, Electrocardiograph |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-02-09 |
Device Publish Date | 2023-02-01 |
10850048235004 | Electrode, Electrocardiograph-40 Pouches of 50 |
00850048235007 | Electrode, electrocardiograph-Pouch of 50 |
00850048235021 | Blood Collection Device-Female Luer Adapter |
00850048235014 | Blood Collection Device-Male Luer Adapter |
00850048235052 | Macro Bore IV extension set with Needle less Y-site and removable needless connector |