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Excess Scaler

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 785-795SIRef 785-795XSI

by LM-Instruments Oy

Identity

Trade Name
Excess Scaler EUDAMED
LMDental FDA UDI
Generic Name
Margin finishing dental file/rasp, reusable FDA UDI
Device Name
Restorative dental hand instrument EUDAMED
Excess Scaler, Restoration FDA UDI
Model / Reference
785-795SI EUDAMED
785-795XSI EUDAMEDFDA UDI
Description
Excess Scaler, Restoration FDA UDI

Identifiers

Primary DI / UDI-DI
06438311220581 EUDAMED
06438311220598 EUDAMEDFDA UDI
Basic UDI-DI
6438311RESTO102Y EUDAMED
Direct Marketing DI
06438311220581 EUDAMED
06438311220598 EUDAMED
FDA Product Code
DZN FDA UDI
EMDN Code
Q01010199 DENTAL RESTORATION DEVICES - OTHER EUDAMED
GMDN Term
Margin finishing dental file/rasp, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.4565 FDA UDI
Market of Registration
Finland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental appliance fabrication material, ceramic

Excess Scaler by LM-Instruments Oy — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, ceramic.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
LM-Instruments Oy
EUDAMED SRN
FI-MF-000006705

Sources (3)

  • EUDAMED 3d8bcd0a-4740-4e6f-acda-a7a10d4e1339 61 fields · synced Jul 15, 2026
  • EUDAMED ac999ef0-7ffa-4bd4-a881-4ccbcc9f8c01 61 fields · synced May 17, 2026
  • FDA UDI 9fce4b97-a720-4d2c-8683-801ab11bfb90 33 fields · synced May 30, 2026