FDA UDI In Commercial Distribution 🇺🇸 United States

QuickVue

DI: 30014613202059 · Model: iFOB Test · QUIDEL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
QuickVue
Primary DI
30014613202059
Version / Model
iFOB Test
Catalog Number
20205
Company Name
QUIDEL CORPORATION
Labeler DUNS
079509836
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-15
Public Version
6
Public Version Date
2023-06-16
Public Version Status
Update
Public Device Record Key
33614867-b9fd-4fcf-bde7-6c62d99c1e53

Device Description

QuickVue iFOB Test Dev Kit 100T

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KHE REAGENT, OCCULT BLOOD

GMDN Terms

Code Name
54532 Faecal occult blood IVD, kit, rapid ICT, clinical

Identifiers

Type ID
Primary 30014613202059

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K021423 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius