| Primary Device ID | 07630031710437 |
| NIH Device Record Key | 71693b1c-8e15-4368-beb4-864a2cd3641c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | P.004 ABUTMENTS |
| Version Model Number | 1 |
| Catalog Number | 024.2370 |
| Company DUNS | 483599259 |
| Company Name | Institut Straumann AG |
| 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)448-8168 |
| info.usa@straumann.com |
| Length | 12 Millimeter |
| Outer Diameter | 5 Millimeter |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07630031710437 [Primary] |
| NHA | ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07630031710437]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-12-07 |
| Device Publish Date | 2015-09-24 |
| 07630031710437 | NC Temporary Abutment, D 5mm, H 12mm, PEEK/TAN |
| 07630031710260 | NC Healing Abutment, customizable, D 5mm, PEEK |
| 07630031708915 | RC Abutment, for bars, Ti |
| 07630031708908 | RC Abutment for bars, gold, H 10mm, Ceramicor® |
| 07630031708144 | NC Abutment, for bars, Ti |
| 07630031708137 | NC Abutment for bars, gold, H 10mm, Ceramicor® |