Primary Device ID | 05391525781556 |
NIH Device Record Key | 31c240da-8a4f-4459-aaed-50cfc05a56a7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Biotronik Passeo-35 HP |
Version Model Number | 8/20/75 |
Catalog Number | 399091 |
Company DUNS | 985021909 |
Company Name | CREAGH MEDICAL LIMITED |
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 | 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 |
Device Size Text, specify | 0 |
Length | 20 Millimeter |
Outer Diameter | 8 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05391525781556 [Primary] |
LIT | Catheter, Angioplasty, Peripheral, Transluminal |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-23 |
05391525781617 | 12/40/75 |
05391525781600 | 10/40/75 |
05391525781594 | 9/40/75 |
05391525781587 | 8/80/75 |
05391525781570 | 8/60/75 |
05391525781563 | 8/40/75 |
05391525781556 | 8/20/75 |
05391525781549 | 7/100/75 |
05391525781532 | 7/60/75 |
05391525781525 | 7/40/75 |
05391525781518 | 7/20/75 |
05391525781501 | 6/100/75 |
05391525781495 | 6/60/75 |
05391525781488 | 6/40/75 |
05391525781471 | 6/20/75 |
05391525781464 | 5/60/75 |
05391525781457 | 5/40/75 |
05391525781440 | 5/20/75 |
05391525781433 | 4/40/75 |
05391525781426 | 4/20/75 |
05391525781419 | 3/40/75 |
05391525781358 | 8/40/40 |
05391525781310 | 7/40/40 |
05391525781273 | 6/40/40 |