Primary Device ID | 08056771101455 |
NIH Device Record Key | e25e3555-a292-4ae4-8701-40b32574e12b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LIAISON Analyzer |
Version Model Number | 9450200 |
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 | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 6514399710 |
info@diasorin.com | |
Phone | 6514399710 |
info@diasorin.com | |
Phone | 6514399710 |
info@diasorin.com | |
Phone | 6514399710 |
info@diasorin.com | |
Phone | 6514399710 |
info@diasorin.com | |
Phone | 6514399710 |
info@diasorin.com | |
Phone | 6514399710 |
info@diasorin.com | |
Phone | 6514399710 |
info@diasorin.com | |
Phone | 6514399710 |
info@diasorin.com | |
Phone | 6514399710 |
info@diasorin.com | |
Phone | 6514399710 |
info@diasorin.com | |
Phone | 6514399710 |
info@diasorin.com | |
Phone | 6514399710 |
info@diasorin.com | |
Phone | 6514399710 |
info@diasorin.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08056771101455 [Primary] |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2022-09-16 |
Device Publish Date | 2018-09-24 |
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