← Back to catalogue

Afterloader Basic Device GammaMedplus 3/24, 127V, Series iX

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref GM84000560

by Varian Medical Systems, Inc.

Identity

Trade Name
Afterloader Basic Device GammaMedplus 3/24, 127V,Series iX EUDAMEDFDA UDI
Generic Name
Remote-afterloading brachytherapy system FDA UDI
Device Name
GammaMedplus iX / GammaMedplus 3/24 iX EUDAMED
Model / Reference
GM84000560 EUDAMEDFDA UDI

Identifiers

Catalog Number
GM84000560 FDA UDI
Primary DI / UDI-DI
00816389027329 EUDAMEDFDA UDI
Basic UDI-DI
089947500201002PE EUDAMED
510(k) Number
K120993 FDA UDI
FDA Product Code
JAQ FDA UDI
EMDN Code
Z11010301 BRACHYTHERAPY RADIATION SYSTEMS EUDAMED
GMDN Term
Remote-afterloading brachytherapy system FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
892.5700 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Afterloader Basic Device GammaMedplus 3/24, 127V, Series iX by Varian Medical Systems, Inc — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000001784
Authorised Representative
Siemens Healthineers Nederland B.V. NL-AR-000000803

Sources (2)

  • EUDAMED 9ac8f97e-aa0e-4b5e-a0db-8caff3a0d3aa 61 fields · synced Jul 9, 2026
  • FDA UDI 0ce488d4-64c0-4f3c-8b90-e704454eb6c3 34 fields · synced May 30, 2026