| Primary Device ID | 04046963973063 |
| NIH Device Record Key | d32eb27a-2c16-4591-8f0c-8da3d021d099 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Isodur® |
| Version Model Number | NK771K |
| Catalog Number | NK771K |
| Company DUNS | 315018218 |
| Company Name | Aesculap 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 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04046963973063 [Primary] |
| OQG | Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-04-06 |
| Device Publish Date | 2015-11-11 |
| 04046963973087 | ISODUR PROSTHESIS HEAD 12/14 40MM XXL |
| 04046963973070 | ISODUR PROSTHESIS HEAD 12/14 40MM XL |
| 04046963973063 | ISODUR PROSTHESIS HEAD 12/14 40MM L |
| 04046963973056 | ISODUR PROSTHESIS HEAD 12/14 40MM M |
| 04046963741211 | ISODUR PROSTHESIS HEAD 8/10 36MM XXL |
| 04046963741204 | ISODUR PROSTHESIS HEAD 8/10 36MM XL |
| 04046963741198 | ISODUR PROSTHESIS HEAD 8/10 36MM L |
| 04046963741181 | ISODUR PROSTHESIS HEAD 8/10 36MM M |
| 04046963741174 | ISODUR PROSTHESIS HEAD 8/10 36MM S |
| 04046963741167 | ISODUR PROSTHESIS HEAD 12/14 36MM XXL |
| 04046963741150 | ISODUR PROSTHESIS HEAD 12/14 36MM XL |
| 04046963741143 | ISODUR PROSTHESIS HEAD 12/14 36MM L |
| 04046963741136 | ISODUR PROSTHESIS HEAD 12/14 36MM M |
| 04046963741129 | ISODUR PROSTHESIS HEAD 12/14 36MM S |
| 04038653304509 | ISODUR PROSTHESIS HEAD 8/10 32MM XXL |
| 04038653304394 | ISODUR PROSTHESIS HEAD 8/10 32MM XL |
| 04038653304387 | ISODUR PROSTHESIS HEAD 8/10 32MM L |
| 04038653304370 | ISODUR PROSTHESIS HEAD 8/10 32MM M |
| 04038653304363 | ISODUR PROSTHESIS HEAD 8/10 32MM S |
| 04038653206728 | ISODUR PROSTHESIS HEAD 8/10 28MM XXL |
| 04038653119974 | ISODUR PROSTHESIS HEAD 12/14 32MM XXL |
| 04038653119967 | ISODUR PROSTHESIS HEAD 12/14 32MM XL |
| 04038653119950 | ISODUR PROSTHESIS HEAD 12/14 32MM L |
| 04038653119943 | ISODUR PROSTHESIS HEAD 12/14 32MM M |
| 04038653119936 | ISODUR PROSTHESIS HEAD 12/14 32MM S |
| 04038653119806 | ISODUR PROSTHESIS HEAD 12/14 28MM XXL |
| 04038653119790 | ISODUR PROSTHESIS HEAD 12/14 28MM XL |
| 04038653119783 | ISODUR PROSTHESIS HEAD 12/14 28MM L |
| 04038653119776 | ISODUR PROSTHESIS HEAD 12/14 28MM M |
| 04038653119769 | ISODUR PROSTHESIS HEAD 12/14 28MM S |
| 04038653119547 | ISODUR PROSTHESIS HEAD 12/14 22.2MM L |
| 04038653119530 | ISODUR PROSTHESIS HEAD 12/14 22.2MM M |
| 04038653117949 | ISODUR PROSTHESIS HEAD 8/10 28MM XL |
| 04038653117932 | ISODUR PROSTHESIS HEAD 8/10 28MM L |
| 04038653117925 | ISODUR PROSTHESIS HEAD 8/10 28MM M |
| 04038653117918 | ISODUR PROSTHESIS HEAD 8/10 28MM S |
| 04038653117864 | ISODUR PROSTHESIS HEAD 8/10 22.2MM L |
| 04038653117857 | ISODUR PROSTHESIS HEAD 8/10 22.2MM M |
| 04038653117840 | ISODUR PROSTHESIS HEAD 8/10 22.2MM S |
| 04046963973049 | ISODUR PROSTHESIS HEAD 12/14 40MM S |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ISODUR 79123542 4333460 Live/Registered |
COMPO EXPERT GmbH 2012-09-20 |
![]() ISODUR 74685996 1983947 Dead/Cancelled |
BASF Aktiengesellschaft 1995-06-08 |
![]() ISODUR 74352592 1801823 Dead/Cancelled |
PETROFER Chemie H.R. Fischer GmbH & Co.KG 1993-05-20 |
![]() ISODUR 73571543 1419195 Dead/Cancelled |
GIULINI CHEMIE GMBH 1985-12-04 |
![]() ISODUR 73387789 1271415 Dead/Cancelled |
BASF Aktiengesellschaft 1982-09-23 |
![]() ISODUR 73380728 not registered Dead/Abandoned |
VEREX LABORATORIES, INC. 1982-08-19 |