Primary Device ID | 37613327055291 |
NIH Device Record Key | 291cfb0a-3365-4529-96da-b952beb8624c |
Commercial Distribution Discontinuation | 2016-12-02 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Fluid Safe |
Version Model Number | 0502100000 |
Catalog Number | 0502-100-000 |
Company DUNS | 187502109 |
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 | false |
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 | 07613327055290 [Primary] |
GS1 | 37613327055291 [Package] Contains: 07613327055290 Package: pack [36 Units] Discontinued: 2016-12-02 Not in Commercial Distribution |
KDQ | BOTTLE, COLLECTION, VACUUM |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-23 |
07613327058123 | Fluid Management System, Weighing System |
07613327058116 | Fluid Management System, Pump Unit |
37613327055840 | Fluid Management System, Integrated Tube Set, Do not use if package is damaged, Keep dry, Keep a |
37613327055291 | 3000 CC, Suction Canister |