QUATTROcare PLUS 2124 A

FDA UDI

Class I (US FDA UDI)

by KaVo Dental GmbH

Identity

Trade Name: QUATTROcare PLUS 2124 A FDA UDI
Generic Name: Dental handpiece maintenance unit FDA UDI
Model / Reference: 1.008.3805 FDA UDI

Identifiers

Catalog Number: PLUS 2124 A FDA UDI
Primary DI / UDI-DI: EKAV100838050 FDA UDI
510(k) Number: K071288 FDA UDI
FDA Product Code: EFB FDA UDI
GMDN Term: Dental handpiece maintenance unit FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental handpiece maintenance unit

QUATTROcare PLUS 2124 A by KaVo Dental GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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BeyesLube — Beyes Dental Canada Inc · Class I

Cleared under the same submission

K071288 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: KaVo Dental GmbH

Sources (1)

FDA UDI 6c8b5e7c-c2b1-404e-b88b-27872f97811f 36 fields · synced Jun 1, 2026