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X-ray Catheters

FDA UDI

Class II (US FDA UDI)

by Nucletron B.V.

Identity

Trade Name
X-ray Catheters FDA UDI
Generic Name
Bronchial brachytherapy system applicator, remote-afterloading FDA UDI
Device Name
X-ray Catheter no.2 FDA UDI
Model / Reference
089402P01-01 FDA UDI
Description
X-ray Catheter no.2 FDA UDI

Identifiers

Primary DI / UDI-DI
08717213043770 FDA UDI
FDA Product Code
JAQ FDA UDI
GMDN Term
Bronchial 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bronchial brachytherapy system applicator, remote-afterloading

X-ray Catheters by Nucletron B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nucletron B.V.

Sources (1)

  • FDA UDI a82bf633-de31-4876-9041-4591314de3a4 34 fields · synced May 30, 2026