OsteoBridge™ IDSF Diaphysis Reducing bushing GB21007
GUDID 04048266000132
TiAl6V4 ELI sterile
Merete GmbH
Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis Diaphysis prosthesis| Primary Device ID | 04048266000132 |
| NIH Device Record Key | 9701b5b6-f241-411c-b197-2644c7dad3b2 |
| Commercial Distribution Discontinuation | 2020-02-11 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | OsteoBridge™ IDSF Diaphysis Reducing bushing |
| Version Model Number | 7 for Spacer 20 |
| Catalog Number | GB21007 |
| 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 |
Customer Support Contacts
Device Dimensions
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
| Outer Diameter | 7 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04048266000132 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K051965
FDA Product Code
| HSB | Rod, Fixation, Intramedullary And Accessories |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-02-12 |
| Device Publish Date | 2015-10-15 |
On-Brand Devices [OsteoBridge™ IDSF Diaphysis Reducing bushing]
| 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 |
Trademark Results [OsteoBridge]
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 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.