Primary Device ID | 00863019000337 |
NIH Device Record Key | 01767415-6bc9-430e-b89a-2cc1b191ed36 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bloom2 |
Version Model Number | Bloom2 Stimulator |
Catalog Number | 370046G |
Company DUNS | 079978232 |
Company Name | Fischer Medical |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00863019000337 [Primary] |
JOQ | Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-02-25 |
Device Publish Date | 2019-01-25 |
00863019000351 | Bloom2 Cardiac Stimulator System: External Programmable Pacemaker Pulse Generator |
00863019000344 | Bloom2 Cardiac Stimulator System: External Programmable Pacemaker Pulse Generator |
00863019000337 | Bloom2 Cardiac Stimulator System: External Programmable Pacemaker Pulse Generator |
00863019000368 | Bloom2 Cardiac Stimulator System: External Programmable Pacemaker Pulse Generator |