FDA UDI In Commercial Distribution 🇺🇸 United States

Validate

DI: 00850011135389 · Model: 207ro · Lgc Clinical Diagnostics, Inc.
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Validate
Primary DI
00850011135389
Version / Model
207ro
Catalog Number
207ro
Company Name
Lgc Clinical Diagnostics, Inc.
Labeler DUNS
075886031
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-14
Public Version
2
Public Version Date
2022-02-24
Public Version Status
Update
Public Device Record Key
130be38f-0995-4f9f-9981-c3f34900a803

Device Description

Validate Body Fluids 3 is intended for quantitative determination of Calibration Verification/Linearity on 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
38224 Cancer antigen 19-9 (CA19-9) IVD, control
38173 Carcinoembryonic antigen (CEA) IVD, control

Identifiers

Type ID
Primary 00850011135389

Customer Contacts

Storage Conditions

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