Primary Device ID | B101150314XU0 |
NIH Device Record Key | 05d39d73-3a9d-4042-a276-20b6ba3a1e75 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BodyGuard® Pole Mount Charger |
Version Model Number | 150-314XU |
Company DUNS | 002125419 |
Company Name | CME AMERICA LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
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 | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx | |
Phone | 303-936-4945 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B101150314XU0 [Primary] |
FRN | Pump, Infusion |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-16 |
B101150314XU0 | 150-314XU |
B101150313XU0 | 150-313XU |