FDA UDI In Commercial Distribution 🇺🇸 United States

HEMOSURE®

DI: 00857338006033 · Model: T1-CK25 · HEMOSURE INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
HEMOSURE®
Primary DI
00857338006033
Version / Model
T1-CK25
Catalog Number
T1-CK25
Company Name
HEMOSURE INC.
Labeler DUNS
806777541
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2016-08-01
Public Version
4
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
4bf426ac-654b-4306-a6dd-e3d8d62566dd

Device Description

Hemosure iFOB Test 25 Cassettes and 25 Collection Tubes per Box Kit without Mailer

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
Yes

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 00857338006033
Unit of Use 00857338006002