Wagner SL Revision® 01.00103.017
GUDID 00889024480216
Zimmer GmbH
Revision uncoated hip femur prosthesis| Primary Device ID | 00889024480216 |
| NIH Device Record Key | 48b223b1-f064-4ff6-812d-4c32c201b155 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Wagner SL Revision® |
| Version Model Number | 01.00103.017 |
| Catalog Number | 01.00103.017 |
| Company DUNS | 488133448 |
| Company Name | Zimmer 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 |
Customer Support Contacts
Device Dimensions
| Length | 305 Millimeter |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024480216 [Primary] |
FDA Product Code
| LZO | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-08-20 |
| Device Publish Date | 2017-07-28 |
On-Brand Devices [Wagner SL Revision®]
| 00889024485372 | 01.00102.622 |
| 00889024485365 | 01.00102.621 |
| 00889024485358 | 01.00102.620 |
| 00889024485341 | 01.00102.619 |
| 00889024485334 | 01.00102.618 |
| 00889024485327 | 01.00102.617 |
| 00889024485310 | 01.00102.615 |
| 00889024485303 | 01.00102.614 |
| 00889024485273 | 01.00102.222 |
| 00889024485266 | 01.00102.221 |
| 00889024485259 | 01.00102.220 |
| 00889024485242 | 01.00102.219 |
| 00889024485235 | 01.00102.218 |
| 00889024485228 | 01.00102.217 |
| 00889024485211 | 01.00102.616 |
| 00889024485204 | 01.00102.216 |
| 00889024485198 | 01.00102.215 |
| 00889024485181 | 01.00102.214 |
| 00889024485174 | 01.00101.920 |
| 00889024485167 | 01.00101.919 |
| 00889024485150 | 01.00101.918 |
| 00889024485143 | 01.00101.917 |
| 00889024485136 | 01.00101.916 |
| 00889024485129 | 01.00101.915 |
| 00889024485112 | 01.00101.914 |
| 00889024480919 | 01.00102.625 |
| 00889024480902 | 01.00102.624 |
| 00889024480896 | 01.00102.623 |
| 00889024480650 | 01.00103.025 |
| 00889024480636 | 01.00103.024 |
| 00889024480612 | 01.00103.023 |
| 00889024480261 | 01.00103.022 |
| 00889024480254 | 01.00103.021 |
| 00889024480247 | 01.00103.020 |
| 00889024480230 | 01.00103.019 |
| 00889024480223 | 01.00103.018 |
| 00889024480216 | 01.00103.017 |
| 00889024480209 | 01.00103.016 |
| 00889024480193 | 01.00103.015 |
| 00889024480179 | 01.00103.014 |
| 00889024430976 | Wagner SL Revision® Hip Stem, uncemented, ø 25/305, taper 12/14 |
| 00889024430969 | Wagner SL Revision® Hip Stem, uncemented, ø 24/305, taper 12/14 |
| 00889024430952 | Wagner SL Revision® Hip Stem, uncemented, ø 23/305, taper 12/14 |
| 00889024430945 | Wagner SL Revision® Hip Stem, uncemented, ø 22/305, taper 12/14 |
| 00889024430938 | Wagner SL Revision® Hip Stem, uncemented, ø 21/305, taper 12/14 |
| 00889024430921 | Wagner SL Revision® Hip Stem, uncemented, ø 20/305, taper 12/14 |
| 00889024430914 | Wagner SL Revision® Hip Stem, uncemented, ø 19/305, taper 12/14 |
| 00889024430907 | Wagner SL Revision® Hip Stem, uncemented, ø 18/305, taper 12/14 |
| 00889024430891 | Wagner SL Revision® Hip Stem, uncemented, ø 17/305, taper 12/14 |
| 00889024430884 | Wagner SL Revision® Hip Stem, uncemented, ø 16/305, taper 12/14 |
Trademark Results [Wagner SL Revision]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 WAGNER SL REVISION 78550022 3122860 Live/Registered |
Zimmer GmbH 2005-01-19 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.