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Kamvac

FDA UDI

Class II (US FDA UDI)

by Depuy Orthopaedics, Inc.

Identity

Trade Name
KAMVAC FDA UDI
Generic Name
Disposable vacuum tubing FDA UDI
Device Name
KAMVAC CURVED MINI SUCTION TUBE FDA UDI
Model / Reference
5300-20-500 FDA UDI
Description
KAMVAC CURVED MINI SUCTION TUBE FDA UDI

Identifiers

Catalog Number
530020500 FDA UDI
Primary DI / UDI-DI
10603295171515 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Disposable vacuum tubing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Disposable vacuum tubing

Kamvac by Depuy Orthopaedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Disposable vacuum tubing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f5cca317-6202-458d-be41-f42bef599c60 35 fields · synced Jun 8, 2026