← Back to catalogue

Guide tube for Ø 2.0 mm needles

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref GM11013410

by Varian Medical Systems, Inc.

Identity

Trade Name
Guide tube for Ø 2.0 mm needles EUDAMED
Guide tube for Ø 2 mm needles FDA UDI
Generic Name
Vaginal brachytherapy system applicator, remote-afterloading FDA UDI
Device Name
Intracavitary/ Interstitial System EUDAMED
Model / Reference
GM11013410 EUDAMEDFDA UDI

Identifiers

Catalog Number
GM11013410 FDA UDI
Primary DI / UDI-DI
00816389027954 EUDAMEDFDA UDI
Basic UDI-DI
089947500201203PS EUDAMED
510(k) Number
K250289 FDA UDI
FDA Product Code
JAQ FDA UDI
EMDN Code
Z11010380 BRACHYTHERAPY RADIATION SYSTEMS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Vaginal brachytherapy system applicator, remote-afterloading FDA UDI

Classification

Device Class
Class IIa 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Safe FDA UDI

Guide tube for Ø 2.0 mm needles by Varian Medical Systems, Inc — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

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 e0006b5b-95c4-46ed-948c-3e7a7e82c172 61 fields · synced Jul 15, 2026
  • FDA UDI 59cd9198-6cdf-400d-9b15-46cc2bc06af5 34 fields · synced May 30, 2026