Primary Device ID | 04035479147143 |
NIH Device Record Key | cc8c106a-118b-41be-bd64-83327d3aad5b |
Commercial Distribution Discontinuation | 2020-10-16 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | PSW |
Version Model Number | 1403.U |
Catalog Number | 406797 |
Company DUNS | 315620229 |
Company Name | BIOTRONIK SE & Co. KG |
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 | false |
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 |
Phone | +1(888)345-0374 |
jon.brumbaugh@biotronik.com | |
Phone | +1(888)345-0374 |
jon.brumbaugh@biotronik.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04035479147143 [Primary] |
OSR | Pacemaker/icd/crt non-implanted components |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-10-19 |
Device Publish Date | 2015-03-15 |
04035479166397 | 1904.U |
04035479157692 | 1703.U |
04035479157678 | 1702.U |
04035479154165 | 1506.U/1 |
04035479152765 | 1507.U |
04035479150204 | 1502.U |
04035479149260 | 1501.U |
04035479147143 | 1403.U |
04035479140670 | 1304.U |
04035479140380 | 1307.U |
04035479151843 | 1506.U |
04035479150211 | 1503.U |
04035479174798 | 2100.U |
04035479160838 | 1801.U |
04035479157708 | 1704.U |
04035479162047 | 1802.U |
04035479164423 | 1901.U |
04035479164416 | 1804.U |
04035479178024 | 2201.U/1 |
04035479181543 | 2301.U |
04035479179632 | 2204.U |
04035479184292 | 2303.U |
04035479186012 | 2401.U |