| Primary Device ID | 04048266000217 |
| NIH Device Record Key | ec523d43-f89f-44af-b6d7-3113e08fda5b |
| Commercial Distribution Discontinuation | 2023-06-01 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | OsteoBridge™ IDSF Diaphysis Reducing bushing |
| Version Model Number | 12 for Spacer 30 |
| Catalog Number | GB21612 |
| Company DUNS | 313267265 |
| Company Name | Merete GmbH |
| 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 | true |
| 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 |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Outer Diameter | 12 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04048266000217 [Primary] |
| HSB | Rod, Fixation, Intramedullary And Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2023-07-04 |
| Device Publish Date | 2015-10-15 |
| 04048266140692 | TiAl6V4 ELI sterile |
| 04048266140685 | TiAl6V4 ELI sterile |
| 04048266140678 | TiAl6V4 ELI sterile |
| 04048266000194 | TiAl6V4 ELI sterile |
| 04048266000187 | TiAl6V4 ELI sterile |
| 04048266000170 | TiAl6V4 ELI sterile |
| 04048266000156 | TiAl6V4 ELI sterile |
| 04048266000149 | TiAl6V4 ELI sterile |
| 04048266000132 | TiAl6V4 ELI sterile |
| 04048266000224 | TiAl6V4 ELI sterile |
| 04048266000217 | TiAl6V4 ELI sterile |
| 04048266000200 | TiAl6V4 ELI sterile |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() OSTEOBRIDGE 86180106 4636001 Live/Registered |
ARISTOTECH INDUSTRIES GMBH 2014-01-30 |
![]() OSTEOBRIDGE 77009670 3354525 Dead/Cancelled |
ARISTOTECH INDUSTRIES GMBH 2006-09-28 |