PreScreen HCG Urine Pregnancy Dip Test

Basic Information

• Brand Name: PreScreen HCG Urine Pregnancy Dip Test
• Primary DI: 00851000007229
• Version / Model: PS-HCG
• Company Name: MERGERS MARKETING, INC.
• Labeler DUNS: 065602744
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2016-12-07
• Public Version: 4
• Public Version Date: 2022-06-10
• Public Version Status: Update
• Public Device Record Key: dee601bb-362a-4cb1-af4f-301e26462771

Device Description

PreScreen HCG Urine Pregnancy Dip Test

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: Yes
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: Yes
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
CHM	Radioimmunoassay, Total Estrogens In Pregnancy	Clinical Chemistry	862.1270	1

GMDN Terms

Code	Name	Definition	Implantable	Status
46994	Multiple drugs of abuse IVD, kit, rapid ICT, clinical	A collection of reagents and other associated materials intended to be used for the qualitative and/or (semi-)quantitative detection of multiple drugs of abuse in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method [lateral flow test]. This is a rapid test used in the laboratory or in point-of-care analyses. It is not intended to be used for self-testing.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	00851000007243	GS1	Case	50	In Commercial Distribution
Package	00851000007236	GS1	Inner Pack	20	In Commercial Distribution
Primary	00851000007229	GS1