Primary Device ID | 37613327055840 |
NIH Device Record Key | 19b693b0-202b-404a-9984-2a413304cb71 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Fluid Safe |
Version Model Number | 0502200000A |
Catalog Number | 0502-200-000A |
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 | 07613327055849 [Primary] |
GS1 | 37613327055840 [Package] Contains: 07613327055849 Package: pack [10 Units] In Commercial Distribution |
HIG | INSUFFLATOR, HYSTEROSCOPIC |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-10-14 |
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 |