Arvolife HCG Midstream
Arvolife HCG Midstream is a Class II device made by Clinical Guard, listed in FDA GUDID since 27 Mar 2018 (UDI-DI 00851950008130), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00851950008130 | Date27 Mar 2018 | StatusListed |
Official records
- AccessGUDID record 00851950008130
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Arvolife
- Generic name
- Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, immunochromatographic test (ICT), rapid
- Model / reference
- HCG Midstream
- Primary DI / UDI-DI
- 00851950008130
- FDA product code
- LCX
- GMDN term
- Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, immunochromatographic test (ICT), rapid
- Device class
- Class II
- Regulation number
- 862.1155
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code LCX (Kit, Test, Pregnancy, Hcg, Over The Counter).
- HUMAN CHORIONIC GONADOTROPIN (HCG) TEST SYSTEM FOR THE EARLY DETECTION OF PREGNANCY by Ml Strategies, Inc.
- CLEARBLUE EASY EARLY RESULT PREGNANCY TEST by Unipath, Ltd.
- Clearblue® Early Digital Pregnancy Test by SPD SWISS PRECISION DIAGNOSTICS GMBH
- BEST PREGNANCY TEST by Ameritek, Inc.
- MIDSTREAM ONESTEP PREGNANCY HOME TEST by SYNTRON BIORESEARCH, INC.
- MODIFIED HOMECLINIC PREGNANCY TEST by Vanguard Biomedical Corp.
- EPT CERTAINTY PREGNANCY TEST by Unipath, Ltd.
- PREGNA/TEST by Modern Diagnostics, Inc.
- C&T PREGNANCY TEST KIT by Healthcheck Corp.
- QUIDEL HOME PREGNANCY TEST by Quidel Corp.