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BladeCARTRIDGE-1

FDA UDI

Class I (US FDA UDI)

by Qlicksmart Pty Ltd

Identity

Trade Name
BladeCARTRIDGE-1 FDA UDI
Generic Name
Scalpel blade remover, sterile 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-1 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
19337363001626 FDA UDI
FDA Product Code
GES FDA UDI
GMDN Term
Scalpel blade remover, sterile 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
Sterilization Method
Radiation Sterilization FDA UDI

Category: Scalpel blade remover, sterile

BladeCARTRIDGE-1 by Qlicksmart Pty Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scalpel blade remover, sterile.

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 56244c1d-fce2-4955-a9d1-389dda6d79e6 34 fields · synced Jun 6, 2026