| Primary Device ID | 20686864054881 |
| NIH Device Record Key | 8845cad3-bfcd-43fd-b9d4-f08f4ff2eaa1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MEDICOM PRO-MATRIX |
| Version Model Number | SP-30010 |
| Catalog Number | SP-30010 |
| Company DUNS | 256880576 |
| Company Name | AMD Medicom Inc |
| Device Count | 2 |
| 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Phone | +1(514)636-6262 |
| amdudi@medicom.ca | |
| Phone | +1(514)636-6262 |
| amdudi@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca | |
| Phone | +1(514)636-6262 |
| mkansou@medicom.ca |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Cool dry place |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00686864054887 [Unit of Use] |
| GS1 | 20686864054881 [Primary] |
| DZN | INSTRUMENTS, DENTAL HAND |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-02-25 |
| Device Publish Date | 2019-01-24 |
| 20686864054881 | MEDICOM CURVED PRO-MATRIX BAND Sample |
| 20686864054874 | MEDICOM CURVED PRO-MATRIX BAND sample |
| 20686864054867 | MEDICOM CURVED PRO-MATRIX BAND 4 mm Narrow |
| 20686864054850 | MEDICOM CURVED PRO-MATRIX BAND 6 mm wide |
| 20686864049832 | MEDICOM PRO-MATRIX BAND 4,5 mm Narrow |