FDA UDI In Commercial Distribution 🇺🇸 United States

ForSure iFOB Test (cassette only)

DI: 00748349000076 · Model: 10210 · SYNTRON BIORESEARCH, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ForSure iFOB Test (cassette only)
Primary DI
00748349000076
Version / Model
10210
Company Name
SYNTRON BIORESEARCH, INC.
Labeler DUNS
174517060
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-29
Public Version
5
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
cc6eebdc-6ba8-49c8-b5f4-28857712b00c

Device Description

ForSure iFOB test cassette only (no buffer)

Device Characteristics

Single Use
Yes
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
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
Package 10748349000073
Primary 00748349000076

Premarket Submissions

Submission Number Supplement Number
K063693 000