FDA UDI In Commercial Distribution 🇺🇸 United States

VALIDATE

DI: 00850011135501 · Model: 402pf · Lgc Clinical Diagnostics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VALIDATE
Primary DI
00850011135501
Version / Model
402pf
Company Name
Lgc Clinical Diagnostics, Inc.
Labeler DUNS
075886031
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-01
Public Version
1
Public Version Date
2022-11-09
Public Version Status
New
Public Device Record Key
d791a095-d302-4406-ada5-6bc505344132

Device Description

VALIDATE 402pf is intended for Calibration Verification / Linearity of cardiac markers in automated instruments.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
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
JJY Multi-Analyte Controls, All Kinds (Assayed)

GMDN Terms

Code Name
47869 Multiple-type clinical chemistry analyte profile IVD, control

Identifiers

Type ID
Primary 00850011135501

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-25 – -10 Degrees Celsius