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Cavex Vibringe

FDA UDI

Class I (US FDA UDI)

by Cavex Holland B.V.

Identity

Trade Name
Cavex Vibringe FDA UDI
Generic Name
Dental irrigation/aspiration syringe FDA UDI
Device Name
Edodontic Irrigating Device FDA UDI
Model / Reference
VI001 FDA UDI
Description
Edodontic Irrigating Device FDA UDI

Identifiers

Catalog Number
VI001 FDA UDI
Primary DI / UDI-DI
E241VI0010 FDA UDI
FDA Product Code
EIC FDA UDI
GMDN Term
Dental irrigation/aspiration syringe FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Dental irrigation/aspiration syringe

Cavex Vibringe by Cavex Holland B.V. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental irrigation/aspiration syringe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cavex Holland B.V.

Sources (1)

  • FDA UDI be508fdc-df55-4b83-8358-95c15b3db031 36 fields · synced Jun 6, 2026