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Small Prostate Brachytherapy Kit

FDA UDI

Class I (US FDA UDI)

by Liberty Medical Inc

Identity

Trade Name
Small Prostate Brachytherapy Kit FDA UDI
Generic Name
Prostate brachytherapy system applicator, manual FDA UDI
Device Name
The prostate brachytherapy kit provides the prostate template and flexineedles used in prostate brachytherapy FDA UDI
Model / Reference
5800 FDA UDI
Description
The prostate brachytherapy kit provides the prostate template and flexineedles used in prostate brachytherapy FDA UDI

Identifiers

Primary DI / UDI-DI
B165580000326083124156 FDA UDI
FDA Product Code
IWJ FDA UDI
GMDN Term
Prostate brachytherapy system applicator, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.5650 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 15 Gauge FDA UDI

Category: Prostate brachytherapy system applicator, manual

Small Prostate Brachytherapy Kit by Liberty Medical Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Prostate brachytherapy system applicator, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Liberty Medical Inc

Sources (1)

  • FDA UDI 30b6ea1c-db09-4525-b35f-e8705d4f1371 34 fields · synced May 30, 2026