Primary Device ID | DO3642013032 |
NIH Device Record Key | b2f1f1a3-a880-436e-a59f-b76329e48aef |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LOJIC+ |
Version Model Number | LOJIC+ 1SP REG 50 |
Catalog Number | 4201303 |
Company DUNS | 753221852 |
Company Name | SDI LIMITED |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +18002285166 |
info@sdi.com.au |
Handling Environment Atmospheric Pressure | Between 0 Degrees Celsius and 25 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
HIBCC | DO3642013030 [Unit of Use] |
HIBCC | DO3642013032 [Primary] |
EJJ | Alloy, amalgam |
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 | 2016-09-23 |
DO3642250002 | LOJIC+ 5SP REG 500 |
DO3642234042 | LOJIC+ 3SP SLOW 500 |
DO3642233032 | LOJIC+ 3SP REG 500 |
DO3642232022 | LOJIC+ 3SP FAST 500 |
DO3642224042 | LOJIC+ 2SP SLOW 500 |
DO3642223032 | LOJIC+ 2SP REG 500 |
DO3642222022 | LOJIC+ 2SP FAST 500 |
DO3642214042 | LOJIC+ 1SP SLOW 500 |
DO3642213032 | LOJIC+ 1SP REG 500 |
DO3642212022 | LOJIC+ 1SP FAST 500 |
DO3642050002 | LOJIC+ 5SP REG 50 |
DO3642034042 | LOJIC+ 3SP SLOW 50 |
DO3642033032 | LOJIC+ 3SP REG 50 |
DO3642032022 | LOJIC+ 3SP FAST 50 |
DO3642024042 | LOJIC+ 2SP SLOW 50 |
DO3642023032 | LOJIC+ 2SP REG 50 |
DO3642022022 | LOJIC+ 2SP FAST 50 |
DO3642014042 | LOJIC+ 1SP SLOW 50 |
DO3642013032 | LOJIC+ 1SP REG 50 |
DO3642012022 | LOJIC+ 1SP FAST 50 |