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Impla Clean Plastic Implant Instrument Kit

FDA UDI

Class I (US FDA UDI)

by Hager Worldwide, Inc.

Identity

Trade Name
Impla Clean Plastic Implant Instrument Kit FDA UDI
Generic Name
Manual dental scaler, reusable FDA UDI
Device Name
Set of four double-ended plastic implant instruments. Each instrument is shaped differently. FDA UDI
Model / Reference
355220 FDA UDI
Description
Set of four double-ended plastic implant instruments. Each instrument is shaped differently. FDA UDI

Identifiers

Primary DI / UDI-DI
D24835522010 FDA UDI
FDA Product Code
EIY FDA UDI
GMDN Term
Manual dental scaler, reusable 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

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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Manual dental scaler, reusable

Impla Clean Plastic Implant Instrument Kit by Hager Worldwide, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual dental scaler, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI efff5cd1-0feb-46bc-a05e-4ed5d4f585dd 34 fields · synced Jun 9, 2026