← Back to catalogue

Dimension Vista® Cuvettes

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Dimension Vista® Cuvettes FDA UDI
Generic Name
Laboratory analyser cuvette IVD, single-use FDA UDI
Device Name
Cuvettes, 20x240 (4800) FDA UDI
Model / Reference
10445211 FDA UDI
Description
Cuvettes, 20x240 (4800) FDA UDI

Identifiers

Catalog Number
KS850 FDA UDI
Primary DI / UDI-DI
00842768016271 FDA UDI
510(k) Number
K051087 FDA UDI
FDA Product Code
JJE FDA UDI
GMDN Term
Laboratory analyser cuvette IVD, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2160 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: Laboratory analyser cuvette IVD, single-use

Dimension Vista® Cuvettes by Siemens Healthcare Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laboratory analyser cuvette IVD, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI 096344e2-f16f-463a-815c-b21d7194d813 37 fields · synced Jun 8, 2026