QuickLink™

FDA UDI

Class II (US FDA UDI)

by Bard Brachytherapy, Inc

Identity

Trade Name: QuickLink™ FDA UDI
Generic Name: General-purpose brachytherapy system applicator, manual FDA UDI
Device Name: QuickLink™ Cartridge 5.5 mm Spacer FDA UDI
Model / Reference: SPCRQC20 FDA UDI
Description: QuickLink™ Cartridge 5.5 mm Spacer FDA UDI

Identifiers

Catalog Number: SPCRQC20 FDA UDI
Primary DI / UDI-DI: 10801741078122 FDA UDI
FDA Product Code: KXK FDA UDI
IWJ FDA UDI
GMDN Term: General-purpose brachytherapy system applicator, manual FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 892.5730 FDA UDI
892.5650 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: General-purpose brachytherapy system applicator, manual Brachytherapy source spacer

QuickLink™ by Bard Brachytherapy, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Bard Brachytherapy, Inc

Sources (1)

FDA UDI 6f727a05-993b-48ec-ba7f-40502cbbd7d7 36 fields · synced May 30, 2026