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Riverpoint Brachytherapy

FDA UDI

Class II (US FDA UDI)

by Riverpoint Medical Llc

Identity

Trade Name
RIVERPOINT BRACHYTHERAPY FDA UDI
Generic Name
Manual brachytherapy source, permanent implant FDA UDI
Device Name
BRACHYTHERAPY FDA UDI
Model / Reference
GM1054K FDA UDI
Description
BRACHYTHERAPY FDA UDI

Identifiers

Primary DI / UDI-DI
00812444023190 FDA UDI
510(k) Number
K103449 FDA UDI
FDA Product Code
NEU FDA UDI
GMDN Term
Manual brachytherapy source, permanent implant FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Manual brachytherapy source, permanent implant

Riverpoint Brachytherapy by Riverpoint Medical Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual brachytherapy source, permanent implant.

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 edd202bc-ac51-409f-b00f-f94e60ea4474 34 fields · synced May 30, 2026