Primary Device ID | 07613327116618 |
NIH Device Record Key | 50e08358-ae0a-46da-8cd1-87d4e83ad835 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Howmedica, Definition |
Version Model Number | 6265004311 |
Catalog Number | 6265004311 |
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 | 07613327116618 [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 |