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Root Canal Excavator 1.5mm

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 632-642ESModel Dental hand instrument, excavator for preparation of root canal

by LM-Instruments Oy

Identity

Trade Name
Root Canal Excavator 1.5mm EUDAMED
LMDental FDA UDI
Generic Name
Dental excavator, reusable FDA UDI
Device Name
Endodontic hand instruments Ir EUDAMED
Root Canal Excavator 1.5mm, Endodontics FDA UDI
Model / Reference
632-642ES EUDAMEDFDA UDI
Dental hand instrument, excavator for preparation of root canal EUDAMED
Description
Root Canal Excavator 1.5mm, Endodontics FDA UDI

Identifiers

Primary DI / UDI-DI
06438311217734 EUDAMEDFDA UDI
Basic UDI-DI
6438311ENDO1r0SD EUDAMED
B-06438311217734 EUDAMED
Direct Marketing DI
06438311217734 EUDAMED
FDA Product Code
DZN FDA UDI
EMDN Code
L159002 DENTAL EXCAVATORS, REUSABLE EUDAMED
GMDN Term
Dental excavator, 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

Yes

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

Root Canal Excavator 1.5mm by LM-Instruments Oy — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

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 a23f5d15-11d9-45d3-876f-314f6c8ec87c 61 fields · synced Jul 18, 2026
  • EUDAMED 2d7d54e8-4366-4501-a6c8-bd761c30a962 61 fields · synced May 17, 2026
  • FDA UDI 8b2c513a-890e-4bc6-994d-a3fa17af112d 33 fields · synced May 30, 2026