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Saline Diluent (ns)

EUDAMEDFDA UDI

Class A (EU MDR)

Ref SA8396

by Randox Laboratories Limited

Identity

Trade Name
SALINE DILUENT (NS) EUDAMED
NS FDA UDI
Generic Name
Isotonic saline reagent IVD FDA UDI
Device Name
SALINE DILUENT EUDAMED
This product should be used in conjunction with RX daytona plus reagents to dilute samples prior to assay. FDA UDI
Model / Reference
SA8396 EUDAMEDFDA UDI
Description
This product should be used in conjunction with RX daytona plus reagents to dilute samples prior to assay. FDA UDI

Identifiers

Catalog Number
SA8396 FDA UDI
Primary DI / UDI-DI
05055273209389 EUDAMEDFDA UDI
Basic UDI-DI
50552732ASALDIL007DT EUDAMED
FDA Product Code
JJE FDA UDI
EMDN Code
W01019001 BUFFERS (UNASSIGNABLE), SUPPLEM. REAGENTS, ETC (CC) EUDAMED
GMDN Term
Isotonic saline reagent IVD 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

Saline Diluent (ns) by Randox Laboratories Limited — 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

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

Manufacturer

EUDAMED SRN
XI-MF-000028410

Sources (2)

  • EUDAMED 3b6a1cc2-631e-4d9b-ad79-d858a9515707 61 fields · synced Jul 25, 2026
  • FDA UDI 07bc9774-137b-4a03-8ec1-e0800c1f92aa 36 fields · synced May 30, 2026