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BladeCARTRIDGE

FDA UDI

Class I (US FDA UDI)

by Qlicksmart Pty Ltd

Identity

Trade Name
BladeCARTRIDGE FDA UDI
Generic Name
Bile duct brachytherapy system applicator, manual FDA UDI
Device Name
BladeCARTRIDGE is available as an add-on to the Qlicksmart BladeNeedleSYSTEM if you need more scalpel blade removers in this needle holder. FDA UDI
Model / Reference
QSSVCAT-1B FDA UDI
Description
BladeCARTRIDGE is available as an add-on to the Qlicksmart BladeNeedleSYSTEM if you need more scalpel blade removers in this needle holder. FDA UDI

Identifiers

Primary DI / UDI-DI
09337363001711 FDA UDI
FDA Product Code
GES FDA UDI
GMDN Term
Bile duct brachytherapy system applicator, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bile duct brachytherapy system applicator, manual

BladeCARTRIDGE by Qlicksmart Pty Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bile duct brachytherapy system applicator, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Qlicksmart Pty Ltd

Sources (1)

  • FDA UDI 3e14b7a5-1a26-47ed-bef3-9e71a2c5c354 34 fields · synced Jun 8, 2026