| Primary Device ID | 04046963124502 |
| NIH Device Record Key | 581540fe-c1d3-4d24-b27e-71d43ad20faa |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AS |
| Version Model Number | NN261Z |
| Catalog Number | NN261Z |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 04046963124502 [Primary] |
| JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-07-30 |
| Device Publish Date | 2015-09-24 |
| 04046964027024 | AS TIBIA EXTENSION STEM D14MM L12MM |
| 04046964027017 | AS TIBIA EXTENSION STEM D12MM L12MM |
| 04046963124519 | AS TIBIAL OBTURATOR D14MM |
| 04046963124502 | AS TIBIAL OBTURATOR D12MM |
| 04046963937874 | AS TIBIA OFFSET STEM D15X172 CEMENTLESS |
| 04046963937454 | AS TIBIA OFFSET STEM D19X172 CEMENTLESS |
| 04046963810559 | AS TIBIA EXTENSION STEM 12X52MM CEMENTED |
| 04046963655846 | AS TIBIA EXTENS.STEM 10X92MM CEMENTLESS |
| 04046963655808 | AS TIBIA EXTENSION STEM 10X52MM CEMENTED |
| 04046963176853 | AS FEMUR EXTENS.STEM 7° D18X177 CEM.LESS |
| 04046963176839 | AS FEMUR EXTENS.STEM 7° D16X177 CEM.LESS |
| 04046963176808 | AS FEMUR EXTENS.STEM 7° D13X177 CEM.LESS |
| 04046963176754 | AS FEMUR EXTENS.STEM 7° D17X117 CEM.LESS |