Home GUDID 06936983167123 Shinetell Digital Pregnancy Test
Primary DI 06936983167123
Brand Shinetell Digital Pregnancy Test
Company Hangzhou AllTest Biotech Co., Ltd.
Model 1
Catalog number FHC-AE103H
Device description 2T, FDA OTC
Published 2026-04-15
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx false
OTC true
Sterile false
Single use true Product Codes# Code, Name table Code Name LCX Kit, Test, Pregnancy, Hcg, Over The Counter
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class LCX Kit, Test, Pregnancy, Hcg, Over The Counter Clinical Chemistry 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 06936983167123 Primary GS1 0 86936983167129 Unit of Use GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 06936983167123 06936983167123 6936983167123 86936983167129 86936983167129
GMDN Terms# Term, Definition table Term Definition Total human chorionic gonadotropin 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 total human chorionic gonadotropin (HCG), which includes a combination of intact HCG, nicked HCG, alpha-HCG subunits, and beta-HCG subunits, 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 to aid detection of pregnancy, or as a predictor of adverse pregnancy outcomes (e.g., miscarriage) and/or trisomy 21 (Down syndrome). It is not intended to be used for self-testing.
Regulatory Flags# DUNS number 543254717 Device count 2 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 16936983131633 Multi-Drug Rapid Test Panel (Urine) 1 DOA-A1104C 2026-04-16 16936983131640 Multi-Drug Rapid Test Panel (Urine) 1 DOA-A1124C 2026-04-16 16936983138632 Multi-Drug 12 Drugs Rapid Test Cup 1 DOA-A1127C-062-b-A3 2026-04-16 16936983141120 Discover Multi-Drug 12 Drugs Rapid Test Cup 1 DUA-A1127C-A3 2026-04-16 16936983141137 Discover Multi-Drug 12 Drugs Rapid Test Cup 1 DUA-A1127C-A3 2026-04-16 16936983144664 Discover DISP-CUP164N$ 2023-11-30 16936983144671 Discover DISP-DUD6144N$ 2023-11-30 16936983144688 Discover Multi-Drug 10 Drugs Rapid Test Cup (Urine) 1 DOA-A1107C-A3 2026-04-16 16936983149744 Discover milti-drug 7 drugs rapid test cup DUA-A177C-A3 A1617 DISP-DUD774N$ 2024-02-08 16936983153819 Discover Multi-Drug 13 Drugs Rapid Test Cup (Urine) 1 DUA-A1137C-A3 2026-04-15 16936983165379 Discover Multi-Drug 5 Drugs Rapid Test Cup(Urine) 1 DUA-A157C-A3 2026-04-15 16936983169599 Alltest Multi-Drug Rapid Urine Test Panel 1 DOA-A1144C-026-b 2026-04-15 16936983169605 Alltest Multi-Drug Rapid Urine Test Panel 1 DUA-A1144C-003-b 2026-04-15 16936983169865 Discover Multi-Drug 6 Drugs Rapid Test Cup (Urine) 1 DUA-A167C-A3 2026-04-15 16936983169872 Discover Multi-Drug 8 Drugs Rapid Test Cup (Urine) 1 DUA-A187C-A3 2026-04-15 16936983170007 Alltest Multi-Drug 12 Drugs Urine Test Panel 1 DOA-A1124C 2026-04-15 16936983170014 Alltest Multi-Drug 13 Drugs Urine Test Panel 1 DOA-A1134C 2026-04-15 16936983170021 Alltest Multi-Drug 14 Drugs Urine Test Panel 1 DOA-A1144C 2026-04-15 16936983170038 Alltest Multi-Drug 14 Drugs Urine Test Panel 1 DOA-A1144C 2026-04-15 16936983171998 Alltest Multi-Drug 13 Drugs Rapid Urine Test Panel 1 DOA-A1134C 2026-04-15
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