Primary Device ID | 10610586045547 |
NIH Device Record Key | 8aa996d6-8ea5-4e50-8115-1a9ca96b07f0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pneupac |
Version Model Number | 123004 |
Company DUNS | 106712748 |
Company Name | SMITHS MEDICAL MD, INC. |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10610586045547 [Primary] |
BTL | Ventilator, emergency, powered (resuscitator) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-11-27 |
Device Publish Date | 2015-09-01 |
30610586045749 | WW122006 |
30610586045558 | 124003 |
10610586045547 | 123004 |
10610586045530 | 123001 |
10610586045523 | 123000 |
10610586045516 | 122203 |
10610586045509 | 122202 |
30610586038284 | 122004 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() PNEUPAC 75758396 2345686 Live/Registered |
SMITHS MEDICAL INTERNATIONAL LIMITED 1999-07-23 |
![]() PNEUPAC 73372613 1295889 Dead/Cancelled |
Pneupac Limited 1982-07-01 |