FDA UDI In Commercial Distribution 🇺🇸 United States

RAPID DIAGNOSTICS HCG TEST CARD

DI: 00817830020272 · Model: 07RD7002 · RAPID DIAGNOSTICS INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RAPID DIAGNOSTICS HCG TEST CARD
Primary DI
00817830020272
Version / Model
07RD7002
Catalog Number
07RD7002
Company Name
RAPID DIAGNOSTICS INC
Labeler DUNS
008028248
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-20
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
7898da0c-644c-44b5-b17a-0743f6a0bf96

Device Description

HCG TEST CARD

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
JHI Visual, pregnancy hCG, prescription use

GMDN Terms

Code Name
54216 Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, immunochromatographic test (ICT), rapid

Identifiers

Type ID
Primary 00817830020272

Customer Contacts

Device Sizes

Type Value Unit Text
Length 72 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius