Primary Device ID | 28056771103415 |
NIH Device Record Key | f5a3da45-55f0-432b-bf59-bd84ee93c0fd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LIAISON XL MUREX Control HBeAg |
Version Model Number | 318151 |
Company DUNS | 630822989 |
Company Name | DIASORIN 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 | 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 | 08056771103411 [Primary] |
GS1 | 28056771103415 [Package] Contains: 08056771103411 Package: [20 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 |
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