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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