← Back to catalogue

AFP, CEA & PSA AccuLite VAST CLIA Kit - 192 wells

EUDAMEDFDA UDI

Class C (EU MDR)

Ref 8475-300BModel 8475-300

by Monobind Inc.

Identity

Trade Name
AFP, CEA & PSA AccuLite VAST CLIA Kit - 192 wells EUDAMED
AFP, CEA, PSA Cancer Panel AccuLite VAST CLIA Test System - 192 Wells FDA UDI
Generic Name
Alpha-fetoprotein (AFP) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
Alpha-Fetoprotein,Carcinoembryonic Antigen and Total Prostate Specific Antigen (AFP/CEA/tPSA) VAST® AccuLite® CLIA Test System EUDAMED
Model / Reference
8475-300 EUDAMEDFDA UDI
8475-300B EUDAMED

Identifiers

Catalog Number
8475-300B FDA UDI
Primary DI / UDI-DI
00816870022109 EUDAMEDFDA UDI
Basic UDI-DI
081687002PSAVAST84752H EUDAMED
FDA Product Code
LOJ FDA UDI
EMDN Code
W0102030112,W0102030122,W0102039001 EUDAMED
GMDN Term
Alpha-fetoprotein (AFP) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class C EUDAMED
Class II FDA UDI
Regulation Number
866.6010 FDA UDI
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

New Device

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 7.75 Inch FDA UDI

AFP, CEA & PSA AccuLite VAST CLIA Kit - 192 wells by Monobind, Inc. — Class C — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Monobind Inc.
EUDAMED SRN
US-MF-000021611
Authorised Representative
CEpartner4U NL-AR-000000111

Sources (2)

  • EUDAMED 88fb91f7-5187-42d6-8498-682a7009a02d 61 fields · synced Jun 19, 2026
  • FDA UDI 979b09c3-bf4b-42c7-be24-96e62f96ca85 36 fields · synced May 27, 2026