Primary Device ID | 07640130447165 |
NIH Device Record Key | 452dac3a-a638-43cd-9f8b-4089f03bdb2e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PK Papyrus |
Version Model Number | 3.0/15/140 |
Catalog Number | 434888 |
Company DUNS | 480862817 |
Company Name | Biotronik AG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 |
Phone | +1(888)345-0374 |
jon.brumbaugh@biotronik.com |
Device Size Text, specify | 0 |
Storage Environment Temperature | Between 50 Degrees Fahrenheit and 77 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07640130447165 [Primary] |
NIV | coronary covered stent |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-10-07 |
Device Publish Date | 2019-04-08 |
07640130447318 | 5.0/26/140 |
07640130447301 | 4.5/26/140 |
07640130447295 | 4.0/26/140 |
07640130447288 | 3.5/26/140 |
07640130447271 | 3.0/26/140 |
07640130447264 | 5.0/20/140 |
07640130447257 | 4.5/20/140 |
07640130447240 | 4.0/20/140 |
07640130447233 | 3.5/20/140 |
07640130447226 | 3.0/20/140 |
07640130447219 | 2.5/20/140 |
07640130447202 | 5.0/15/140 |
07640130447196 | 4.5/15/140 |
07640130447189 | 4.0/15/140 |
07640130447172 | 3.5/15/140 |
07640130447165 | 3.0/15/140 |
07640130447158 | 2.5/15/140 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PK PAPYRUS 86382931 4839556 Live/Registered |
BIOTRONIK AG 2014-09-02 |