← Back to catalogue

TripleAngled BA Excavator3.5mm

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 671-681XSIModel Dental hand instrument, excavator for the removal of softened carious dentin

by LM-Instruments Oy

Identity

Trade Name
TripleAngled BA Excavator3.5mm EUDAMED
LMDental FDA UDI
Generic Name
Dental excavator, reusable FDA UDI
Device Name
Restorative hand instrument Ir EUDAMED
TripleAngled BA Excavator 3.5mm, Restoration FDA UDI
Model / Reference
Dental hand instrument, excavator for the removal of softened carious dentin EUDAMED
671-681XSI EUDAMEDFDA UDI
Description
TripleAngled BA Excavator 3.5mm, Restoration FDA UDI

Identifiers

Primary DI / UDI-DI
06438311036717 EUDAMEDFDA UDI
Basic UDI-DI
B-06438311036717 EUDAMED
6438311RESTO1r0C6 EUDAMED
Direct Marketing DI
06438311036717 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

TripleAngled BA Excavator3.5mm by LM-Instruments Oy — Class I — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (3)

  • EUDAMED 43429408-f7cd-4b8c-a236-c1357ca848e1 61 fields · synced Jul 11, 2026
  • EUDAMED 54110a21-85b9-4658-9e7d-712a64ef4e09 61 fields · synced May 17, 2026
  • FDA UDI e3b67c17-fdc0-4851-aef2-b40881482054 33 fields · synced May 29, 2026