Primary Device ID | 10840861101983 |
NIH Device Record Key | 48520d32-e909-47d1-ab18-2209af286820 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Liberty® PDx |
Version Model Number | 050-87221 |
Catalog Number | 050-87221 |
Company DUNS | 958291411 |
Company Name | Fresenius Medical Care Holdings, Inc. |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)323-5188 |
xxx@xxx.xxx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840861101986 [Primary] |
GS1 | 10840861101983 [Package] Contains: 00840861101986 Package: Case [10 Units] In Commercial Distribution |
FKX | SYSTEM, PERITONEAL, AUTOMATIC DELIVERY |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2015-10-02 |
10840861101990 | Liberty® PDx Cycler Integrated Set |
10840861101983 | Liberty® PDx Cycler Set with Single stay.safe® PIN Connector |
10840861101976 | Liberty® PDx Cycler Set with Dual stay.safe® PIN Connectors |