FDA UDI In Commercial Distribution 🇺🇸 United States

LIAISON® XL

DI: 08056771102148 · Model: I0050 · DIASORIN SPA
Product Codes
0
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LIAISON® XL
Primary DI
08056771102148
Version / Model
I0050
Company Name
DIASORIN SPA
Labeler DUNS
630822989
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
671fdb00-8da4-4ed6-9eda-d0df05b744a6

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

GMDN Terms

Code Name
56701 Chemiluminescent immunoassay analyser IVD

Identifiers

Type ID
Primary 08056771102148

Customer Contacts

Phone
651-439-9710