Primary Device ID | 04048266179784 |
NIH Device Record Key | dc45872d-7b71-46d3-bf4b-648a7afa5a9d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OsteoBridge™ IDSF Diaphysis Humeral Spacer |
Version Model Number | 20 50 |
Catalog Number | GB60002S |
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 | 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 |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 20 Millimeter |
Length | 50 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04048266179784 [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 | 2 |
Public Version Date | 2023-05-08 |
Device Publish Date | 2018-10-31 |
04048266179807 | 20 70 |
04048266179791 | 20 60 |
04048266179784 | 20 50 |
04048266179777 | 20 40 |
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 |