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Varian Verification Console

FDA UDI

Class II (US FDA UDI)

by Varian Medical Systems India Software Private Limited

Identity

Trade Name
Varian Verification Console FDA UDI
Generic Name
Radiation therapy treatment record/verify system FDA UDI
Model / Reference
2.3 FDA UDI

Identifiers

Primary DI / UDI-DI
00856104006123 FDA UDI
510(k) Number
K124002 FDA UDI
FDA Product Code
LHN FDA UDI
GMDN Term
Radiation therapy treatment record/verify system 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

No

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: Radiation therapy treatment record/verify system

Varian Verification Console by Varian Medical Systems India Software Private Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiation therapy treatment record/verify system.

Cleared under the same submission

K124002 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
Varian Medical Systems India Software Private Limited

Sources (1)

  • FDA UDI 3eb2f067-3bb1-4606-93ad-4cff4cd15798 33 fields · synced May 30, 2026