← Back to catalogue

WASH BUFFER CONCENTRATE (BUF WASH (conc.))

EUDAMEDFDA UDI

Class A (EU MDR)

Ref EV3581

by Randox Laboratories Limited

Identity

Trade Name
WASH BUFFER CONCENTRATE (BUF WASH (conc.)) EUDAMED
BUF WASH (conc.) FDA UDI
Generic Name
Wash/cleaning solution IVD, automated/semi-automated system FDA UDI
Device Name
WASH BUFFER CONCENTRATE (BUF WASH (conc.)) EUDAMED
Diluted wash buffer is used for washing the biochips between assay steps to remove all unbound materials. FDA UDI
Model / Reference
EV3581 EUDAMEDFDA UDI
Description
Diluted wash buffer is used for washing the biochips between assay steps to remove all unbound materials. FDA UDI

Identifiers

Catalog Number
EV3581 FDA UDI
Primary DI / UDI-DI
05055273202663 EUDAMEDFDA UDI
Basic UDI-DI
50552732ABUFWAS021GL EUDAMED
510(k) Number
K030360 FDA UDI
FDA Product Code
JJE FDA UDI
EMDN Code
W0201020185 AUTOMATED IMMUNOCHEMISTRY ANALYSERS - CONSUMABLES EUDAMED
GMDN Term
Wash/cleaning solution IVD, automated/semi-automated system FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
862.2160 FDA UDI
Market of Registration
Northern Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

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

WASH BUFFER CONCENTRATE (BUF WASH (conc.)) by Randox Laboratories Limited — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID

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
Randox Laboratories Limited
EUDAMED SRN
XI-MF-000028410

Sources (2)

  • EUDAMED 27bc0e4c-f9e0-404b-bdd0-2b2e8afb5b7a 61 fields · synced Jul 12, 2026
  • FDA UDI 0bc9a48b-52b1-43d9-a92b-6d2d11705c15 37 fields · synced May 30, 2026