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Novoste Response Kit

FDA UDI

Class III (US FDA UDI)

by Best Vascular, Inc.

Identity

Trade Name
Novoste Response Kit FDA UDI
Generic Name
Manual-afterloading brachytherapy system utility kit FDA UDI
Device Name
Response Kit for Novoste Beta-Cath System FDA UDI
Model / Reference
RSK-0002 FDA UDI
Description
Response Kit for Novoste Beta-Cath System FDA UDI

Identifiers

Catalog Number
RSK-0002 FDA UDI
Primary DI / UDI-DI
M097RSK00020 FDA UDI
PMA Number
P000018 FDA UDI
FDA Product Code
MOU FDA UDI
GMDN Term
Manual-afterloading brachytherapy system utility kit FDA UDI

Classification

Device Class
Class III 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: Manual-afterloading brachytherapy system utility kit

Novoste Response Kit by Best Vascular, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual-afterloading brachytherapy system utility kit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Best Vascular, Inc.

Sources (1)

  • FDA UDI 05d9994c-c33f-4c28-9b02-686bd88553f0 36 fields · synced Jun 8, 2026