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CarboJet® CO2 Bone Lavage System

FDA UDI

Class II (US FDA UDI)

by Kinamed, Inc.

Identity

Trade Name
CarboJet® CO2 Bone Lavage System FDA UDI
Generic Name
Bone cleaning gas-jet nozzle, reusable FDA UDI
Device Name
Angle Nozzle FDA UDI
Model / Reference
25-200-0220 FDA UDI
Description
Angle Nozzle FDA UDI

Identifiers

Catalog Number
25-200-0220 FDA UDI
Primary DI / UDI-DI
00898142001487 FDA UDI
FDA Product Code
FQH FDA UDI
GMDN Term
Bone cleaning gas-jet nozzle, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5475 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone cleaning gas-jet nozzle, reusable

CarboJet® CO2 Bone Lavage System by Kinamed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone cleaning gas-jet nozzle, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kinamed, Inc.

Sources (1)

  • FDA UDI a0424488-dbee-4ad7-93a3-f8bd2e68d8ac 34 fields · synced May 30, 2026