Primary Device ID | 37613154805465 |
NIH Device Record Key | d5938fcd-0515-4083-86c7-ef8c51144481 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 0206501000 |
Catalog Number | 0206501000 |
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 |
Angle | 90 degree |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613154805464 [Primary] |
GS1 | 37613154805465 [Package] Contains: 07613154805464 Package: pack [6 Units] In Commercial Distribution |
JDZ | MIXER, CEMENT, FOR CLINICAL USE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-10-25 |
Device Publish Date | 2018-09-24 |
07613327578577 - Target Tetra | 2024-10-08 Detachable Coil |
07613327578584 - Target Tetra | 2024-10-08 Detachable Coil |
07613327578591 - Target Tetra | 2024-10-08 Detachable Coil |
07613327578607 - Target Tetra | 2024-10-08 Detachable Coil |
07613327578614 - Target Tetra | 2024-10-08 Detachable Coil |
07613327578621 - Target Tetra | 2024-10-08 Detachable Coil |
07613327578638 - Target Tetra | 2024-10-08 Detachable Coil |
07613327578645 - Target Tetra | 2024-10-08 Detachable Coil |