FDA UDI In Commercial Distribution 🇺🇸 United States

BioPlex 2200

DI: 00847865002295 · Model: SW4V3 · BIO-RAD LABORATORIES, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BioPlex 2200
Primary DI
00847865002295
Version / Model
SW4V3
Catalog Number
6653265D
Company Name
BIO-RAD LABORATORIES, INC.
Labeler DUNS
884513334
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-12
Public Version
4
Public Version Date
2021-07-29
Public Version Status
Update
Public Device Record Key
e7ab8920-e52e-40dd-b649-5d6683771f3a

Device Description

U.S. IFU, Manual & CDs, Anti-CCP IFU, SW4_v3

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NHX ANTIBODIES, ANTI-CYCLIC CITRULLINATED PEPTIDE (CCP)
JJY Multi-analyte controls, all kinds (assayed)
JIX CALIBRATOR, MULTI-ANALYTE MIXTURE

GMDN Terms

Code Name
54897 Cyclic citrullinated peptide antibody (anti-CCP) IVD, kit, multiplex

Identifiers

Type ID
Primary 00847865002295

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 1 Each