← Back to catalogue

Probe unit

FDA UDI

Class II (US FDA UDI)

by Scibase AB

Identity

Trade Name
Probe unit FDA UDI
Generic Name
Neoplasm electrical impedance spectrometer FDA UDI
Device Name
Used with the Nevisense to perform lesion examinations on patients, using disposable electrodes attached to the probe. FDA UDI
Model / Reference
512-0003 FDA UDI
Description
Used with the Nevisense to perform lesion examinations on patients, using disposable electrodes attached to the probe. FDA UDI

Identifiers

Catalog Number
512-0003 FDA UDI
Primary DI / UDI-DI
07350094440088 FDA UDI
PMA Number
P150046 FDA UDI
FDA Product Code
ONV FDA UDI
GMDN Term
Neoplasm electrical impedance spectrometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.1820 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Neoplasm electrical impedance spectrometer

Probe unit by Scibase AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neoplasm electrical impedance spectrometer.

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

Manufacturer
Scibase AB

Sources (1)

  • FDA UDI 06bf45e1-e5f2-4405-9adb-35ac0ad8f72f 35 fields · synced May 30, 2026