← Back to catalogue

NOVIUS Lab

FDA UDI

Class I (US FDA UDI)

by Cerner Corporation

Identity

Trade Name
NOVIUS Lab FDA UDI
Generic Name
Clinical laboratory information system application software FDA UDI
Device Name
Laboratory Information System application software FDA UDI
Model / Reference
27.2.2 FDA UDI
Description
Laboratory Information System application software FDA UDI

Identifiers

Primary DI / UDI-DI
00853023006159 FDA UDI
FDA Product Code
JQP FDA UDI
GMDN Term
Clinical laboratory information system application software FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2100 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

NOVIUS Lab by Cerner Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Manufacturer
Cerner Corporation

Sources (1)

  • FDA UDI 1b855576-781e-4267-a260-4e583c114167 34 fields · synced May 31, 2026