← Back to catalogue

EPIgray

FDA UDI

Class II (US FDA UDI)

by Dosisoft SA

Identity

Trade Name
EPIgray FDA UDI
Generic Name
Radiation therapy software FDA UDI
Device Name
Radiotherapy quality assurance software tool. FDA UDI
Model / Reference
2.0.10 FDA UDI
Description
Radiotherapy quality assurance software tool. FDA UDI

Identifiers

Catalog Number
EP1001 FDA UDI
Primary DI / UDI-DI
B501EPIGRAY020010 FDA UDI
510(k) Number
K112723 FDA UDI
FDA Product Code
MUJ FDA UDI
GMDN Term
Radiation therapy software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5050 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

No

FDA UDI

Category: Radiation therapy software

EPIgray by Dosisoft SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiation therapy software.

Cleared under the same submission

K112723 also covers:

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
Dosisoft SA

Sources (1)

  • FDA UDI 0193b8ce-b377-48cf-b1fe-dc3957b6001b 35 fields · synced Jun 6, 2026