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N Diluent

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
N Diluent FDA UDI
Generic Name
Buffered sample diluent IVD FDA UDI
Device Name
Solution for preparing dilutions for immunochemical determinations with the Dimension Vista® System FDA UDI
Model / Reference
10469513 FDA UDI
Description
Solution for preparing dilutions for immunochemical determinations with the Dimension Vista® System FDA UDI

Identifiers

Catalog Number
OUMT05 FDA UDI
Primary DI / UDI-DI
00842768030239 FDA UDI
510(k) Number
K860894 FDA UDI
FDA Product Code
CFN FDA UDI
GMDN Term
Buffered sample diluent IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5510 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Category: Buffered sample diluent IVD

N Diluent by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Buffered sample diluent IVD.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4414d821-3279-4770-af6e-3fb63cd6a156 37 fields · synced May 30, 2026