| Primary Device ID | 00889024275737 |
| NIH Device Record Key | cc51eeb8-7c24-45b3-9dcb-59a7acbfb272 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ANATOMICAL SHOULDER™ DOMELOCK® |
| Version Model Number | 01.04558.213 |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024275737 [Primary] |
| KWS | PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
[00889024275737]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-10-14 |
| Device Publish Date | 2016-09-24 |
| 00889024485297 | 01.04212.505 |
| 00889024485280 | 01.04212.485 |
| 00889024485006 | 01.04227.005 |
| 00889024480469 | 01.04213.565 |
| 00889024480452 | 01.04212.565 |
| 00889024480445 | 01.04213.545 |
| 00889024480438 | 01.04212.545 |
| 00889024480421 | 01.04213.525 |
| 00889024480414 | 01.04212.525 |
| 00889024480407 | 01.04213.505 |
| 00889024480391 | 01.04213.485 |
| 00889024480384 | 01.04213.465 |
| 00889024480377 | 01.04212.465 |
| 00889024480360 | 01.04213.445 |
| 00889024480353 | 01.04212.445 |
| 00889024480346 | 01.04213.425 |
| 00889024480339 | 01.04212.425 |
| 00889024480322 | 01.04213.405 |
| 00889024480315 | 01.04212.405 |
| 00889024480308 | 01.04213.385 |
| 00889024480292 | 01.04212.385 |
| 00889024480285 | 01.04213.365 |
| 00889024480278 | 01.04212.365 |
| 00889024480643 | 01.04227.229 |
| 00889024480605 | 01.04227.219 |
| 00889024480575 | 01.04227.233 |
| 00889024480483 | 01.04227.215 |
| 00889024480698 | 01.04227.227 |
| 00889024480681 | 01.04227.232 |
| 00889024480674 | 01.04227.217 |
| 00889024480667 | 01.04227.222 |
| 00889024480629 | 01.04227.234 |
| 00889024480599 | 01.04227.224 |
| 00889024480582 | 01.04227.228 |
| 00889024480568 | 01.04227.218 |
| 00889024480551 | 01.04227.223 |
| 00889024480544 | 01.04227.226 |
| 00889024480537 | 01.04227.231 |
| 00889024480520 | 01.04227.216 |
| 00889024480513 | 01.04227.221 |
| 00889024480506 | 01.04227.225 |
| 00889024480490 | 01.04227.230 |
| 00889024480476 | 01.04227.220 |
| 00889024387195 | Trial Head 40-17 |
| 00889024387188 | Trial Head 40-14 |
| 00889024276031 | Rasp adapter |
| 00889024276024 | Angle Identification Card right |
| 00889024276017 | Angle Identification Card left |
| 00889024276000 | Trial T-Dome 132R10 / 138L10 - eccentric |
| 00889024275997 | Trial T-Dome 132L10 / 138R10 - eccentric |