FDA UDI In Commercial Distribution 🇺🇸 United States

EXENT® Diluent 1

DI: 05051700020640 · Model: IK876 · THE BINDING SITE GROUP LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
EXENT® Diluent 1
Primary DI
05051700020640
Version / Model
IK876
Company Name
THE BINDING SITE GROUP LIMITED
Labeler DUNS
347045614
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-27
Public Version
1
Public Version Date
2025-12-05
Public Version Status
New
Public Device Record Key
290dc021-b309-4c68-8616-0c150c26256d

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OTA Mass Spectrometer For Clinical Multiplex Test Systems

GMDN Terms

Code Name
58237 Buffered sample diluent IVD

Identifiers

Type ID
Primary 05051700020640

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 25 Degrees Celsius