| Primary Device ID | 00872320000615 |
| NIH Device Record Key | 2415b0bc-c2fa-42dc-8b8a-017fda1b0c8f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FE Scrub Tip |
| Version Model Number | 01859 |
| Company DUNS | 102422578 |
| Company Name | CAO GROUP, INC. |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 877-236-4408 |
| info@caogroup.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00872320000608 [Package] Contains: 00872320004378 Package: Pack [25 Units] In Commercial Distribution |
| GS1 | 00872320000615 [Package] Contains: 00872320004378 Package: Pack [50 Units] In Commercial Distribution |
| GS1 | 00872320004378 [Primary] |
| KXR | Applicator, Resin |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-11-08 |
| Device Publish Date | 2018-09-21 |
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