Primary Device ID | 37613327055208 |
NIH Device Record Key | f852e53a-0b2d-4d4f-b650-c5b6178a1cda |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CrossFlow |
Version Model Number | 0450000100 |
Catalog Number | 0450-000-100 |
Company DUNS | 187502109 |
Company Name | STRYKER CORPORATION |
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 |
Phone | +1(866)624-4422 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327055207 [Primary] |
GS1 | 37613327055208 [Package] Contains: 07613327055207 Package: pack [10 Units] In Commercial Distribution |
HRX | ARTHROSCOPE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-04-23 |
Device Publish Date | 2016-09-23 |
37613327261036 | Patient-Use Tubing, Do not use if package is damaged |
37613327261029 | Day-Use Inflow Cassette Tubing, Do not use if package is damaged |
07613327058079 | Stryker Console Customizer |
07613327058062 | Footswitch |
07613327058048 | Integrated Arthroscopy Pump |
37613327055222 | Integrated Cassette Tubing, Do not use if package is damaged |
37613327055215 | Outflow Cassette Tubing, Do not use if package is damaged |
37613327055208 | Inflow Cassette Tubing, Do not use if package is damaged |