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HCG URINE CONTROL Negative/Low Positive 2x4mL KITBOX

EUDAMEDFDA UDI

Class IVD General (EU MDR)

Ref 702013

by Biochemical Diagnostics, Inc

Identity

Trade Name
HCG URINE CONTROL Negative/Low Positive 2x4mL KITBOX EUDAMED
Pregnancy-Skreen FDA UDI
Generic Name
Human chorionic gonadotropin beta-core fragment IVD, control FDA UDI
Device Name
PREGNANCY-SKREEN hCG LIQUID CONTROLS EUDAMED
Kova poc, Pregnancy-Skreen hcG Liquid Control Urine, Negative and Positive Control, 5mL Kitbox FDA UDI
Model / Reference
702013 EUDAMEDFDA UDI
Description
Kova poc, Pregnancy-Skreen hcG Liquid Control Urine, Negative and Positive Control, 5mL Kitbox FDA UDI

Identifiers

Catalog Number
702013 FDA UDI
Primary DI / UDI-DI
00850004812242 EUDAMEDFDA UDI
Basic UDI-DI
B-00850004812242 EUDAMED
FDA Product Code
JJX FDA UDI
EMDN Code
W05039099 DEVICES FOR SAMPLES ANALYSES - OTHER EUDAMED
GMDN Term
Human chorionic gonadotropin beta-core fragment IVD, control FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Class I FDA UDI
Regulation Number
862.1660 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

HCG URINE CONTROL Negative/Low Positive 2x4mL KITBOX by Biochemical Diagnostics Inc — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000025179
Authorised Representative
Advena Limited MT-AR-000000234

Sources (2)

  • EUDAMED 71962af6-ccb8-4276-adce-60e810f639d9 61 fields · synced Jul 14, 2026
  • FDA UDI b994b7d2-7a82-4b38-a7ac-5a8a62195199 36 fields · synced May 30, 2026