Primary Device ID | DO3685001001 |
NIH Device Record Key | 063fe097-d25f-4e32-ad95-d6ed5f684643 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ROK |
Version Model Number | ROK SYR INTRO KT |
Catalog Number | 8500100 |
Company DUNS | 753221852 |
Company Name | SDI LIMITED |
Device Count | 1 |
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 | true |
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 10 Degrees Celsius and 25 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
HIBCC | DO3685001001 [Primary] |
EBF | MATERIAL, TOOTH SHADE, RESIN |
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 | 2016-09-30 |
DO3685001011 | ROK SHADE GUIDE 5 SYR KT |
DO3685001001 | ROK SYR INTRO KT |
DO3685000111 | ROK 1 SYR C2 |
DO3685000071 | ROK 1 SYR B2 |
DO3685000061 | ROK 1 SYR B1 |
DO3685000041 | ROK 1 SYR A3.5 |
DO3685000031 | ROK 1 SYR A3 |
DO3685000021 | ROK 1 SYR A2 |