Primary Device ID | DO3686505101 |
NIH Device Record Key | 8231b5d8-5e89-4a8d-a44c-f525561da8b3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RIVA LUTING |
Version Model Number | RIVA LUTING P/L TRIPLE PK |
Catalog Number | 8650510 |
Company DUNS | 753221852 |
Company Name | SDI LIMITED |
Device Count | 3 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | false |
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 5 Degrees Celsius and 25 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
HIBCC | DO3686505100 [Unit of Use] |
HIBCC | DO3686505101 [Primary] |
EMA | CEMENT, DENTAL |
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 | 2016-10-07 |
DO3686519001 | RIVA LUTING PLUS LQD REF 10G |
DO3686515081 | RIVA LUTING PLUS P/L KT |
DO3686511081 | RIVA LUTING PLUS PWD REF 25G |
DO3686510081 | RIVA LUTING PLUS 50 CAP |
DO3686509001 | RIVA LUTING LQD REF 25G |
DO3686505101 | RIVA LUTING P/L TRIPLE PK |
DO3686505081 | RIVA LUTING P/L KT LARGE |
DO3686501081 | RIVA LUTING LY PWD REF 35 |
DO3686500081 | RIVA LUTING LY 50 CAP |