Primary Device ID | 37613327055635 |
NIH Device Record Key | c4297b82-233e-4c34-a630-0a2a9a88290e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pneumosure |
Version Model Number | 0620040660 |
Catalog Number | 0620-040-660 |
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 | 07613327055634 [Primary] |
GS1 | 37613327055635 [Package] Contains: 07613327055634 Package: pack [10 Units] In Commercial Distribution |
HIF | INSUFFLATOR, LAPAROSCOPIC |
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 | 2016-09-23 |
07613327063295 | XL High Flow Insufflator |
07613327063219 | High Flow Insufflator |
37613327055659 | [High Flow Insufflator, Do not use if package is damaged, Keep dry, Keep away from sunlight, |
37613327055642 | [High Flow Insufflator, Do not use if package is damaged, Keep dry, Keep away from sunlight, |
37613327055635 | [High Flow Insufflator, Do not use if package is damaged, Keep dry, Keep away from sunlight, |
07613327147964 | [Tubeset Adapter for PNEUMO SURE High Flow Insufflator. Do Not Use if Package is Damaged, Keep |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PNEUMOSURE 77015814 3450071 Dead/Cancelled |
Stryker Corporation 2006-10-06 |