FDA UDI In Commercial Distribution 🇺🇸 United States

Liquichek

DI: 00847661001348 · Model: 725 · BIO-RAD LABORATORIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Liquichek
Primary DI
00847661001348
Version / Model
725
Catalog Number
725
Company Name
BIO-RAD LABORATORIES, INC.
Labeler DUNS
051624070
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-14
Public Version
2
Public Version Date
2023-01-31
Public Version Status
Update
Public Device Record Key
f2d758b7-a17d-451d-bf28-e7953a7d2198

Device Description

Liquichek Therapeutic Drug Monitoring Control (TDM) Level 1 (A human serum assayed TDM control.)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
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
DIF Drug mixture control materials

GMDN Terms

Code Name
55235 Multiple-therapy therapeutic drug monitoring IVD, control

Identifiers

Type ID
Primary 00847661001348

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K012741 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-70 – -20 Degrees Celsius