| Primary Device ID | DO3685000021 |
| NIH Device Record Key | 1cc9d058-ad86-4ccb-b236-c85c3f52e005 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ROK |
| Version Model Number | ROK 1 SYR A2 |
| Catalog Number | 8500002 |
| 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 | false |
| 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 10 Degrees Celsius and 25 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | DO3685000021 [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 | 2016-09-29 |
| 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 |