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QuickKart Procedure Cart

FDA UDI

Class II (US FDA UDI)

by Hydrocision, Inc.

Identity

Trade Name
QuickKart Procedure Cart FDA UDI
Generic Name
Water jet knife system handpiece, single-use FDA UDI
Device Name
QuickKart Procedure Cart FDA UDI
Model / Reference
50300 FDA UDI
Description
QuickKart Procedure Cart FDA UDI

Identifiers

Catalog Number
50300 FDA UDI
Primary DI / UDI-DI
00853235007296 FDA UDI
510(k) Number
K002764 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Water jet knife system handpiece, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 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

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

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: Water jet knife system handpiece, single-use

QuickKart Procedure Cart by Hydrocision, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Water jet knife system handpiece, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hydrocision, Inc.

Sources (1)

  • FDA UDI 848d5fda-97c1-4752-973d-90cfa32d47e4 35 fields · synced May 30, 2026