← Back to catalogue

Twin Transport Case

FDA UDI

Class III (US FDA UDI)

by Best Vascular, Inc.

Identity

Trade Name
Twin Transport Case FDA UDI
Generic Name
Manual-afterloading brachytherapy system source transfer device transport case/set FDA UDI
Device Name
Twin Transport Case for the Novoste Beta-Cath System FDA UDI
Model / Reference
TRC-0002 FDA UDI
Description
Twin Transport Case for the Novoste Beta-Cath System FDA UDI

Identifiers

Catalog Number
TRC-0002 FDA UDI
Primary DI / UDI-DI
M097TRC00020 FDA UDI
PMA Number
P000018 FDA UDI
FDA Product Code
MOU FDA UDI
GMDN Term
Manual-afterloading brachytherapy system source transfer device transport case/set 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 source transfer device transport case/set

Twin Transport Case by Best Vascular, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Best Vascular, Inc.

Sources (1)

  • FDA UDI 05d2ef2b-e8f7-41e9-ada9-21c8d59259a1 36 fields · synced May 30, 2026