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Guide tube, Ø 2.8 mm, length 900 mm, front open

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref GM11003180

by Varian Medical Systems, Inc.

Identity

Trade Name
Guide tube, Ø 2.8 mm, length 900 mm, front open EUDAMED
Guide tube 2.8mm diameter, length 900 mm, front open FDA UDI
Generic Name
Tongue brachytherapy system applicator, remote-afterloading FDA UDI
Device Name
Intraluminal Applicator Set EUDAMED
Model / Reference
GM11003180 EUDAMEDFDA UDI

Identifiers

Catalog Number
GM11003180 FDA UDI
Primary DI / UDI-DI
00816389022485 EUDAMEDFDA UDI
Basic UDI-DI
089947500201093QB EUDAMED
510(k) Number
K151022 FDA UDI
FDA Product Code
JAQ FDA UDI
EMDN Code
Z11010380 BRACHYTHERAPY RADIATION SYSTEMS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Tongue 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

No

FDA UDI

Manufacturing Date

No

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

Guide tube, Ø 2.8 mm, length 900 mm, front open by Varian Medical Systems, Inc — Class IIa — 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 c9f02718-a05d-4258-9cd1-6ccf872b0c52 61 fields · synced Jul 17, 2026
  • FDA UDI 9d6b8727-32ee-48fe-8a00-543dae752099 34 fields · synced May 30, 2026