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Hermes Medical Imaging Suite

FDA UDI

Class II (US FDA UDI)

by Hermes Medical Solutions AB

Identity

Trade Name
Hermes Medical Imaging Suite FDA UDI
Generic Name
Nuclear medicine system workstation FDA UDI
Device Name
Hermes Medical Imaging Suite provides software applications used to process, display, analyze and manage nuclear medicine and other medical imaging data transferred from other workstation or acquisition stations. FDA UDI
Model / Reference
6 FDA UDI
Description
Hermes Medical Imaging Suite provides software applications used to process, display, analyze and manage nuclear medicine and other medical imaging data transferred from other workstation or acquisition stations. FDA UDI

Identifiers

Catalog Number
P0 FDA UDI
Primary DI / UDI-DI
00859873006158 FDA UDI
FDA Product Code
KPS FDA UDI
GMDN Term
Nuclear medicine system workstation FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1200 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nuclear medicine system workstation

Hermes Medical Imaging Suite by Hermes Medical Solutions AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nuclear medicine system workstation.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b2a63827-5be7-4a4c-8070-3d44841bbe45 34 fields · synced May 29, 2026