Primary Device ID | 07332414106119 |
NIH Device Record Key | 81e5db08-8470-4e38-b2ad-1dc52c510448 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EXALIS |
Version Model Number | 6041909 |
Catalog Number | 6041909 |
Company DUNS | 428788780 |
Company Name | GAMBRO DASCO SPA |
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 | true |
Manufacturing Date | true |
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 Issuing Agency | Device ID |
---|---|
GS1 | 07332414106119 [Primary] |
KDI | Dialyzer, high permeability with or without sealed dialysate system |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-12-17 |
Device Publish Date | 2018-11-14 |
07332414106126 | Exalis is an integrated product able to acquire, process and supply data required when running a |
07332414106119 | Exalis is an integrated product able to acquire, process and supply data required when running a |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EXALIS 76317630 2674356 Live/Registered |
GAMBRO LUNDIA AB 2001-09-26 |
EXALIS 76317629 2692388 Live/Registered |
GAMBRO LUNDIA AB 2001-09-26 |