Primary Device ID | 10813623017068 |
NIH Device Record Key | 3710c98f-84c2-4b0e-9346-640e183dae4f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ASEPT Peritoneal Drainage System |
Version Model Number | M7008 |
Catalog Number | M7008 |
Company DUNS | 097736867 |
Company Name | PFM MEDICAL INCORPORATED |
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 | true |
Device Combination Product | true |
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 | 7607588749 |
regulatory@pfmmedicalusa.com | |
Phone | 7607588749 |
regulatory@pfmmedicalusa.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00813623017061 [Primary] |
GS1 | 10813623017068 [Package] Contains: 00813623017061 Package: [5 Units] In Commercial Distribution |
FJS | Catheter, Peritoneal, Long-Term Indwelling |
PNG | Peritoneal, Drainage Catheter For Refractory Ascites, Long-Term Indwelling |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-09-06 |
Device Publish Date | 2015-10-15 |
10813623019109 | ASEPT 2,000mL Drainage Bag |
10813623017068 | ASEPT Peritoneal Drainage System |
10813623015378 | ASEPT 1,000mL Drainage Kit |
10813623014227 | ASEPT Drainage Bag with Procedure Pack |
10813623011158 | ASEPT Peritoneal Drainage System |
10813623011141 | ASEPT 1,000mL Drainage Kit |
20813623011117 | ASEPT Vented Lock Cap |