FDA UDI In Commercial Distribution 🇺🇸 United States

BioPlex 2200

DI: 03610520652770 · Model: 12000651 · BIO-RAD LABORATORIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BioPlex 2200
Primary DI
03610520652770
Version / Model
12000651
Catalog Number
12000651
Company Name
BIO-RAD LABORATORIES, INC.
Labeler DUNS
884513334
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-25
Public Version
5
Public Version Date
2020-01-23
Public Version Status
Update
Public Device Record Key
57b6fcb0-1a7b-441e-a869-1330db8f6e1b

Device Description

BioPlex 2200 Syphilis Total & RPR Calibrator Set

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JIT Calibrator, secondary

GMDN Terms

Code Name
51806 Treponema pallidum immunoglobulin G (IgG) antibody IVD, calibrator

Identifiers

Type ID
Primary 03610520652770

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 0.5 Milliliter
Device Size Text, specify 5 Vials

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius