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DELFIA Diluent 3

EUDAMEDFDA UDI

Class A (EU MDR)

Ref 4022-0010

by Wallac Oy

Identity

Trade Name
DELFIA Diluent 3 EUDAMEDFDA UDI
Generic Name
Buffered sample diluent IVD FDA UDI
Device Name
DELFIA Diluent 3 EUDAMED
For use with the AutoDELFIA® and the DELFIA® kits for sample dilution. FDA UDI
Model / Reference
4022-0010 EUDAMEDFDA UDI
Description
For use with the AutoDELFIA® and the DELFIA® kits for sample dilution. FDA UDI

Identifiers

Catalog Number
4022-0010 FDA UDI
Primary DI / UDI-DI
06438147244898 EUDAMEDFDA UDI
Basic UDI-DI
6438147D/AD_Diluent33B EUDAMED
FDA Product Code
PPM FDA UDI
EMDN Code
W01029003 BUFFERS (UNASSIGNABLE), SUPPLEM. REAGENTS, ETC (IC) EUDAMED
GMDN Term
Buffered sample diluent IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
864.4010 FDA UDI
Market of Registration
Finland 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

DELFIA Diluent 3 by Wallac Oy — Class A — 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

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Manufacturer

Manufacturer
Wallac Oy
EUDAMED SRN
FI-MF-000022620

Sources (2)

  • EUDAMED e6e51e0e-1d57-4ef9-9b83-cb043c113d83 61 fields · synced Jun 18, 2026
  • FDA UDI 4ca665bc-7ebc-469c-9849-9075b04e7ee1 35 fields · synced May 29, 2026