| 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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