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Accurun 1 Series 5100 positive control

EUDAMEDFDA UDI

Class IVD General (EU MDR)

Ref 2000-0016

by LGC Clinical Diagnostics, Inc.

Identity

Trade Name
Accurun 1 Series 5100 positive control EUDAMED
ACCURUN® FDA UDI
Generic Name
Multiple blood-borne virus antigen/antibody IVD, control FDA UDI
Device Name
Accurun 1 Series 5100 positive control EUDAMED
ACCURUN 1 Series 5100 Multi-Marker Positive Control 3 x 5.0 mL FDA UDI
Model / Reference
2000-0016 EUDAMEDFDA UDI
Description
ACCURUN 1 Series 5100 Multi-Marker Positive Control 3 x 5.0 mL FDA UDI

Identifiers

Catalog Number
2000-0016 FDA UDI
Primary DI / UDI-DI
00816784020765 EUDAMEDFDA UDI
Basic UDI-DI
B-00816784020765 EUDAMED
FDA Product Code
KSF FDA UDI
EMDN Code
W0105080807 MULTICONSTITUENT CONTROLS - INF.IMM. EUDAMED
GMDN Term
Multiple blood-borne virus antigen/antibody IVD, control FDA UDI

Classification

Device Class
Class IVD General EUDAMED
Class II FDA UDI
Regulation Number
864.9650 FDA UDI
Market of Registration
Ireland 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

Yes

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

Yes

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

No

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

Dimensions & Sizes

Size
Total Volume — 15 Milliliter FDA UDI

A comprehensive medical device directory listing the Accurun 1 Series 5100 positive control, including its specifications, features, and compliance information.

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-000016356
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (2)

  • EUDAMED 02df3d6b-2128-4ec2-963a-49fb8e2a18ff 61 fields · synced Sep 18, 2026
  • FDA UDI aac43b74-4f0d-49c0-9942-5057ba0641fe 37 fields · synced May 30, 2026