← Back to catalogue

Vaginal CT/MR Multi Channel Applicator

FDA UDI

Class II (US FDA UDI)

by Nucletron B.V.

Identity

Trade Name
Vaginal CT/MR Multi Channel Applicator FDA UDI
Generic Name
Cervical/intrauterine brachytherapy system applicator, remote-afterloading FDA UDI
Device Name
Catheter with collar 6Fx293 FDA UDI
Model / Reference
110802-01 FDA UDI
Description
Catheter with collar 6Fx293 FDA UDI

Identifiers

Primary DI / UDI-DI
08717213053724 FDA UDI
510(k) Number
K111973 FDA UDI
FDA Product Code
JAQ FDA UDI
GMDN Term
Cervical/intrauterine 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 6.0 French FDA UDI
Length — 293.0 Millimeter FDA UDI

Category: Cervical/intrauterine brachytherapy system applicator, remote-afterloading

Vaginal CT/MR Multi Channel Applicator by Nucletron B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cervical/intrauterine brachytherapy system applicator, remote-afterloading.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Nucletron B.V.

Sources (1)

  • FDA UDI b9f94ac4-3366-49e7-94d3-f099dc700f10 36 fields · synced May 30, 2026