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Front segment, 20 mm diameter, distal source position

FDA UDI

Class II (US FDA UDI)

by Varian Medical Systems Deutschland GmbH

Identity

Trade Name
Front segment, 20 mm diameter, distal source position FDA UDI
Generic Name
Vaginal brachytherapy system applicator, remote-afterloading FDA UDI
Model / Reference
GM11005260 FDA UDI

Identifiers

Catalog Number
GM11005260 FDA UDI
Primary DI / UDI-DI
00816389023581 FDA UDI
510(k) Number
K033371 FDA UDI
FDA Product Code
JAQ FDA UDI
GMDN Term
Vaginal brachytherapy system applicator, remote-afterloading FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5700 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 20 Millimeter FDA UDI

Category: Vaginal brachytherapy system applicator, remote-afterloading

Front segment, 20 mm diameter, distal source position by Varian Medical Systems Deutschland GmbH — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Vaginal brachytherapy system applicator, remote-afterloading.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7440d692-37fd-4669-9b3e-0ef3da42638e 35 fields · synced May 30, 2026