FDA UDI In Commercial Distribution 🇺🇸 United States

QBC Diagnostics

DI: 00858092006406 · Model: 4237-300-001 · DRUCKER DIAGNOSTICS
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
200

Basic Information

Brand Name
QBC Diagnostics
Primary DI
00858092006406
Version / Model
4237-300-001
Company Name
DRUCKER DIAGNOSTICS
Labeler DUNS
022156957
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
ae542736-d087-4d57-a8f3-d38ad764084f

Device Description

Venous Tube - Blood Collection Device (200 Tube Box); Inner Labeled Package of Venous 1000 Test Kit (424237) *NOT A SOLD PRODUCT*

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
35770 Capillary blood collection tube IVD, no additive

Identifiers

Type ID
Primary 00858092006406
Unit of Use 00858092006369