FDA UDI In Commercial Distribution 🇺🇸 United States

Validate

DI: 00859110005043 · Model: 301ri · Lgc Clinical Diagnostics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Validate
Primary DI
00859110005043
Version / Model
301ri
Catalog Number
301ri
Company Name
Lgc Clinical Diagnostics, Inc.
Labeler DUNS
075886031
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2022-02-24
Public Version Status
Update
Public Device Record Key
78b8d290-a1a1-42e2-87fd-e4b12516f4d2

Device Description

Validate TDM1ri is intended for the quantitative determination of Calibration Verification/Linearity of drug analytes on automated instruments.

Device Characteristics

Single Use
Yes
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
No
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
DKB Calibrators, Drug Mixture

GMDN Terms

Code Name
30503 Multiple therapeutic drugs/drugs of abuse IVD, control

Identifiers

Type ID
Primary 00859110005043

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K033879 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 2 tests

Storage Conditions

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