| Primary Device ID | 00652221287489 |
| NIH Device Record Key | 6874fa4f-6f3b-46ff-b670-3ce75b88d59d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 3M™ APC™ Flash-Free |
| Version Model Number | EXD-959 |
| Catalog Number | EXD-959 |
| Company DUNS | 830016148 |
| Company Name | 3M COMPANY |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 | +1(800)423-4588 |
| 3Mhealthcarecompliance@mmm.com | |
| Phone | +1(800)423-4588 |
| 3Mhealthcarecompliance@mmm.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00652221287489 [Primary] |
| NJM | Bracket, ceramic, orthodontic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-07-23 |
| Device Publish Date | 2018-06-20 |
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