Primary Device ID | 04053755190690 |
NIH Device Record Key | d0bb5507-9074-429e-b15f-2a83f85e68eb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HEINE GAMMA® XXL LF |
Version Model Number | 166 |
Catalog Number | M-000.09.323 |
Company DUNS | 315274563 |
Company Name | Heine Optotechnik GmbH & Co. KG |
Device Count | 1 |
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 | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +1(800)643-6275 |
support@midmark.com | |
Phone | +1(800)643-6275 |
support@midmark.com | |
Phone | +1(800)643-6275 |
support@midmark.com | |
Phone | +1(800)643-6275 |
support@midmark.com | |
Phone | +1(800)643-6275 |
support@midmark.com | |
Phone | +1(800)643-6275 |
support@midmark.com | |
Phone | +1(800)643-6275 |
support@midmark.com | |
Phone | +1(800)643-6275 |
support@midmark.com | |
Phone | +1(800)643-6275 |
support@midmark.com | |
Phone | +1(800)643-6275 |
support@midmark.com | |
Phone | +1(800)643-6275 |
support@midmark.com | |
Phone | +1(800)643-6275 |
support@midmark.com | |
Phone | +1(800)643-6275 |
support@midmark.com | |
Phone | +1(800)643-6275 |
support@midmark.com | |
Phone | +1(800)643-6275 |
support@midmark.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04053755190690 [Primary] |
DXN | System, Measurement, Blood-Pressure, Non-Invasive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-11-03 |
04053755190690 | 166 |
04053755136605 | 000 |
04053755136575 | 000 |