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Athena GTX Device Management Suite (ADMS) Software

FDA UDI

Class II (US FDA UDI)

by Athena Gtx

Identity

Trade Name
Athena GTX Device Management Suite (ADMS) Software FDA UDI
Generic Name
Centralized patient monitor FDA UDI
Device Name
Athena GTX Device Management Suite - Android FDA UDI
Model / Reference
ADMS Android Software FDA UDI
Description
Athena GTX Device Management Suite - Android FDA UDI

Identifiers

Catalog Number
395-0010-00 FDA UDI
Primary DI / UDI-DI
B3943950010000 FDA UDI
510(k) Number
K173203 FDA UDI
FDA Product Code
DRG FDA UDI
MLD FDA UDI
DQA FDA UDI
DXN FDA UDI
DSI FDA UDI
MWI FDA UDI
MHX FDA UDI
MSX FDA UDI
GMDN Term
Centralized patient monitor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2910 FDA UDI
870.1025 FDA UDI
870.2700 FDA UDI
870.1130 FDA UDI
870.2300 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: Centralized patient monitor

Athena GTX Device Management Suite (ADMS) Software by Athena Gtx — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Centralized patient monitor.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Athena Gtx

Sources (1)

  • FDA UDI 5ddaa500-4768-4766-bee9-982ca3bb6e9c 36 fields · synced May 31, 2026