Primary Device ID | 30641043586000 |
NIH Device Record Key | f8bfb420-c0a9-4d24-95e3-1513b9f29471 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CPR-2 Bag |
Version Model Number | 10-58600 |
Company DUNS | 032705659 |
Company Name | MERCURY ENTERPRISES, 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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | (727) 573-0088 |
hospitalcustomerservice@mercurymed.com | |
Phone | (727) 573-0088 |
hospitalcustomerservice@mercurymed.com | |
Phone | (727) 573-0088 |
hospitalcustomerservice@mercurymed.com | |
Phone | (727) 573-0088 |
hospitalcustomerservice@mercurymed.com | |
Phone | (727) 573-0088 |
hospitalcustomerservice@mercurymed.com | |
Phone | (727) 573-0088 |
hospitalcustomerservice@mercurymed.com | |
Phone | (727) 573-0088 |
hospitalcustomerservice@mercurymed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10641043586006 [Primary] |
GS1 | 30641043586000 [Package] Contains: 10641043586006 Package: [6 Units] In Commercial Distribution |
BTM | Ventilator, Emergency, Manual (Resuscitator) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-06-02 |
Device Publish Date | 2018-10-31 |