Primary Device ID | 07613327058116 |
NIH Device Record Key | d901bf4d-da9c-408a-9374-95c3568fd545 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Fluid Safe |
Version Model Number | 0502000001 |
Catalog Number | 0502-000-001 |
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 | false |
Lot Batch | false |
Serial Number | true |
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 |