FDA UDI In Commercial Distribution 🇺🇸 United States

QBC Diagnostics

DI: 00858092006390 · Model: 424240 · DRUCKER DIAGNOSTICS
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
QBC Diagnostics
Primary DI
00858092006390
Version / Model
424240
Catalog Number
424240
Company Name
DRUCKER DIAGNOSTICS
Labeler DUNS
022156957
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-24
Public Version
5
Public Version Date
2023-10-25
Public Version Status
Update
Public Device Record Key
dbae4148-c8e4-464c-89b4-4a39e4ef3fb2

Device Description

Venous Tube - Blood Collection Device (100 Test Kit)

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
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
GIO Tube, Collection, Capillary Blood

GMDN Terms

Code Name
57892 Capillary blood collection tube IVD, K2EDTA

Identifiers

Type ID
Primary 00858092006390
Unit of Use 00858092006369