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Aatma

FDA UDI

Class II (US FDA UDI)

by Elekta Solutions AB

Identity

Trade Name
AATMA FDA UDI
Generic Name
Radiological PACS software FDA UDI
Model / Reference
AATMA FDA UDI

Identifiers

Primary DI / UDI-DI
07340201500040 FDA UDI
510(k) Number
K212218 FDA UDI
FDA Product Code
QKB FDA UDI
LLZ FDA UDI
GMDN Term
Radiological PACS software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Radiological PACS software

Aatma by Elekta Solutions AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiological PACS software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elekta Solutions AB

Sources (1)

  • FDA UDI 15a8d9e9-718b-4429-9589-1a8a5390746f 33 fields · synced May 29, 2026