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Aarhus vaginal template 60°, Ø 32mm

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref GM11013810

by Varian Medical Systems, Inc.

Identity

Trade Name
Aarhus vaginal template 60°, Ø 32mm EUDAMED
Aarhus Vaginal Template 60, Ø32mm FDA UDI
Generic Name
Cervical/intrauterine brachytherapy system applicator, remote-afterloading FDA UDI
Device Name
Aarhus Applicator Set EUDAMED
Aarhus Vaginal Template 60°, Ø32mm FDA UDI
Model / Reference
GM11013810 EUDAMEDFDA UDI
Description
Aarhus Vaginal Template 60°, Ø32mm FDA UDI

Identifiers

Catalog Number
GM11013810 FDA UDI
Primary DI / UDI-DI
00816389028036 EUDAMEDFDA UDI
Basic UDI-DI
089947500201176QG EUDAMED
510(k) Number
K222775 FDA UDI
FDA Product Code
JAQ FDA UDI
EMDN Code
Z11010380 BRACHYTHERAPY RADIATION SYSTEMS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Cervical/intrauterine 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Dry Heat Sterilization FDA UDI
MRI Safety
MR Safe FDA UDI

Aarhus vaginal template 60°, Ø 32mm 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

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Manufacturer

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

Sources (2)

  • EUDAMED afb87709-7829-4bef-8a16-046ac2324215 61 fields · synced Jul 9, 2026
  • FDA UDI 5421d5be-dec5-4b38-b088-af9b75c8851d 35 fields · synced May 30, 2026