| Primary Device ID | 00841396183546 |
| NIH Device Record Key | 48b7034d-86f2-44f7-96f5-584695751581 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Maxcem Elite |
| Version Model Number | 36664 |
| Catalog Number | 36664 |
| Company DUNS | 199354556 |
| Company Name | Kerr Corporation |
| Device Count | 100 |
| 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 | 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 | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com | |
| Phone | 8005377123 |
| customercare@kavokerrgroup.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00008005377123 [Unit of Use] |
| GS1 | 00841396105180 [Unit of Use] |
| GS1 | 00841396183546 [Primary] |
| MZW | Dental Cement W/Out Zinc-Oxide Eugenol As An Ulcer Covering For Pain Relief |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2018-01-22 |
| 00841396183546 | 36664 |
| 00841396108068 | Self-Etch / Self-Adhesive Resin Cement; Intro Kit: 2 syringes Clear, 1 syringe White |
| 00841396107238 | Self-Etch / Self-Adhesive Resin Cement; Sample (NA) - Not For Resale |
| 10841396105255 | Universal Resin Cement ; Bulk Pack |
| 10841396105224 | Universal Resin Cement; Refill Kit; Brown |
| 10841396105217 | Universal Resin Cement with Cleanup Indicator; Refill Kit; Yellow |
| 10841396105200 | Universal Resin Cement; Refill Kit; White Opaque |
| 10841396105194 | Universal Resin Cement; Refill Kit; White |
| 10841396105187 | Universal Resin Cement; Refill Kit; Clear |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MAXCEM ELITE 86902615 5346910 Live/Registered |
Kerr Corporation 2016-02-09 |