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Procedure Accessory Pack, 3.5F Coronary System, 5-Pack

FDA UDI

Class III (US FDA UDI)

by Best Vascular, Inc.

Identity

Trade Name
Procedure Accessory Pack, 3.5F Coronary System, 5-Pack FDA UDI
Generic Name
Manual-afterloading brachytherapy system source delivery procedure kit FDA UDI
Device Name
Five Pack of Procedure Accessory Pack for 3.5F Coronary System FDA UDI
Model / Reference
PAP-0035 FDA UDI
Description
Five Pack of Procedure Accessory Pack for 3.5F Coronary System FDA UDI

Identifiers

Catalog Number
PAP-0035 FDA UDI
Primary DI / UDI-DI
M097PAP00351 FDA UDI
PMA Number
P000018 FDA UDI
FDA Product Code
MOU FDA UDI
GMDN Term
Manual-afterloading brachytherapy system source delivery procedure kit FDA UDI

Classification

Device Class
Class III 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

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-afterloading brachytherapy system source delivery procedure kit

Procedure Accessory Pack, 3.5F Coronary System, 5-Pack 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 source delivery procedure 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 982a1ecf-b46d-4e70-9206-46fbee37e1fa 36 fields · synced Jun 6, 2026