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PDR quick connector socket, 06-10, patient side

FDA UDI

Class II (US FDA UDI)

by Varian Medical Systems Deutschland GmbH

Identity

Trade Name
PDR quick connector socket, 06-10, patient side FDA UDI
Generic Name
Brachytherapy system remote afterloading source transfer tube FDA UDI
Model / Reference
GM11007140 FDA UDI

Identifiers

Catalog Number
GM11007140 FDA UDI
Primary DI / UDI-DI
00816389024014 FDA UDI
510(k) Number
K141336 FDA UDI
FDA Product Code
JAQ FDA UDI
GMDN Term
Brachytherapy system remote afterloading source transfer tube 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

Category: Brachytherapy system remote afterloading source transfer tube

PDR quick connector socket, 06-10, patient side by Varian Medical Systems Deutschland GmbH — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Brachytherapy system remote afterloading source transfer tube.

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 4cd2b58a-b0ad-4f19-90b4-6e34d5745ce6 34 fields · synced May 30, 2026