FDA UDI In Commercial Distribution 🇺🇸 United States

Pregnancy-Skreen

DI: 00850004812242 · Model: 702013 · BIOCHEMICAL DIAGNOSTICS INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Pregnancy-Skreen
Primary DI
00850004812242
Version / Model
702013
Catalog Number
702013
Company Name
BIOCHEMICAL DIAGNOSTICS INC
Labeler DUNS
028007698
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-06
Public Version
2
Public Version Date
2022-08-30
Public Version Status
Update
Public Device Record Key
b994b7d2-7a82-4b38-a7ac-5a8a62195199

Device Description

Kova poc, Pregnancy-Skreen hcG Liquid Control Urine, Negative and Positive Control, 5mL Kitbox

Device Characteristics

Single Use
No
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
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

GMDN Terms

Code Name
42729 Human chorionic gonadotropin beta-core fragment IVD, control

Identifiers

Type ID
Primary 00850004812242

Customer Contacts

Phone
631-595-9200

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius