Primary Device ID | 18056771500187 |
NIH Device Record Key | cdc6f21b-1a0b-452c-99bf-012a3c60d037 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LIAISON XL MUREX HBsAg Qual |
Version Model Number | 318250 |
Company DUNS | 216357118 |
Company Name | DIASORIN S.P.A. |
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 | false |
Single Use | false |
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 Issuing Agency | Device ID |
---|---|
GS1 | 08056771500180 [Primary] |
GS1 | 18056771500187 [Package] Contains: 08056771500180 Package: [10 Units] In Commercial Distribution |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-04-21 |
Device Publish Date | 2021-04-13 |
18056771500200 - LIAISON XL MUREX HIV Ab/Ag HT | 2021-05-12 |
18056771500231 - LIAISON XL MUREX Control HIV Ab/Ag HT | 2021-05-12 |
28056771103583 - LIAISON XL MUREX HBsAg Confirmatory | 2021-04-21 |
18056771500187 - LIAISON XL MUREX HBsAg Qual | 2021-04-21 |
18056771500187 - LIAISON XL MUREX HBsAg Qual | 2021-04-21 |
28056771500214 - LIAISON XL MUREX Control HBsAg Qual | 2021-04-21 |
08056771500197 - LIAISON® XL MUREX HCV Ab | 2020-03-04 |
08056771500227 - LIAISON® XL MUREX Control HCV Ab | 2020-03-04 |