| Primary Device ID | 04546540263179 |
| NIH Device Record Key | 9f61467f-4aca-4339-b219-38ffb8a390dd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Howmedica, Definition |
| Version Model Number | 6265004301 |
| Catalog Number | 6265004301 |
| Company DUNS | 196548481 |
| Company Name | STRYKER CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com |
| Special Storage Condition, Specify | Between 0 and 0 *Store in Cool Dry Place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in Cool Dry Place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in Cool Dry Place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in Cool Dry Place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in Cool Dry Place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in Cool Dry Place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in Cool Dry Place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in Cool Dry Place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in Cool Dry Place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in Cool Dry Place |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04546540263179 [Primary] |
| JDZ | MIXER, CEMENT, FOR CLINICAL USE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2018-09-24 |
| 07613327116618 | Femoral Pressuring Seal Size 4-7 |
| 04546540263179 | Femoral Pressuring Seal Size 1-4 |