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Riverpoint Brachytherapy

FDA UDI

by Riverpoint Medical Llc

Identity

Trade Name
RIVERPOINT BRACHYTHERAPY FDA UDI
Generic Name
Brachytherapy injection needle FDA UDI
Device Name
Brachytherapy FDA UDI
Model / Reference
1200-1810-25 FDA UDI
Description
Brachytherapy FDA UDI

Identifiers

Primary DI / UDI-DI
00812444020441 FDA UDI
GMDN Term
Brachytherapy injection needle FDA UDI

Classification

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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Category: Brachytherapy injection needle

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

Similar devices

Also classified as Brachytherapy injection needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 95723c45-41d7-4b5c-bedb-c80946926eb3 33 fields · synced May 30, 2026