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ORAL-SKREEN NEGATIVE, 500mL

EUDAMEDFDA UDI

Class IVD General (EU MDR)

Ref 20200100

by Biochemical Diagnostics, Inc

Identity

Trade Name
ORAL-SKREEN NEGATIVE, 500mL EUDAMED
SALIVABUSE FDA UDI
Generic Name
Multiple drugs of abuse IVD, control FDA UDI
Device Name
SALIVABUSE LIQUID CONTROL ORAL FLUID EUDAMED
NEGATIVE, 500mL FDA UDI
Model / Reference
20200100 EUDAMEDFDA UDI
Description
NEGATIVE, 500mL FDA UDI

Identifiers

Catalog Number
20200100 FDA UDI
Primary DI / UDI-DI
00810042682573 EUDAMEDFDA UDI
Basic UDI-DI
B-00810042682573 EUDAMED
FDA Product Code
DIF FDA UDI
EMDN Code
W05039099 DEVICES FOR SAMPLES ANALYSES - OTHER EUDAMED
GMDN Term
Multiple drugs of abuse IVD, control FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Class I FDA UDI
Regulation Number
862.3280 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

No

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

ORAL-SKREEN NEGATIVE, 500mL by Biochemical Diagnostics Inc — Class IVD General — IVDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDD

United States Pending data

FDA UDI

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Manufacturer

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

Sources (2)

  • EUDAMED 5a90bed8-0db2-4ea7-8e8e-5e24b81fc6ca 61 fields · synced Jul 9, 2026
  • FDA UDI 1111de84-0deb-4160-ac14-3a0efc9fbb8a 36 fields · synced May 30, 2026