FDA UDI In Commercial Distribution 🇺🇸 United States

hema-screen

DI: 10722355001002 · Model: HS-50 · IMMUNOSTICS COMPANY, INC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
50

Basic Information

Brand Name
hema-screen
Primary DI
10722355001002
Version / Model
HS-50
Company Name
IMMUNOSTICS COMPANY, INC
Labeler DUNS
119214195
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
aa026bb3-1827-407c-a66d-5655c209382b

Device Description

Fecal Occult Blood IVD, Guaiac

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
54531 Faecal occult blood IVD, kit, rapid colorimetric, clinical

Identifiers

Type ID
Package 20722355001009
Primary 10722355001002
Package 30722355001006
Unit of Use 80722355001001

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Keep away from heat and light. Do not refrigerate.