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Gingival margin trimmer, mesial 1, 2mm DTS

EUDAMEDFDA UDI

Class I (EU MDR)

Ref S125-126ESTGREYModel Dental hand instrument, gingival margin for the finishing of cavity

by LM-Instruments Oy

Identity

Trade Name
Gingival margin trimmer, mesial 1,2mm DTS EUDAMED
LMDental FDA UDI
Generic Name
Dental excavator, reusable FDA UDI
Device Name
Restorative hand instrument Ir EUDAMED
Gingival margin trimmer, mesial 1,2mm DTS FDA UDI
Model / Reference
S125-126ESTGREY EUDAMEDFDA UDI
Dental hand instrument, gingival margin for the finishing of cavity EUDAMED
Description
Gingival margin trimmer, mesial 1,2mm DTS FDA UDI

Identifiers

Primary DI / UDI-DI
06438311227429 EUDAMEDFDA UDI
Basic UDI-DI
6438311RESTO1r0C6 EUDAMED
B-06438311227429 EUDAMED
Direct Marketing DI
06438311227429 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

Gingival margin trimmer, mesial 1, 2mm DTS 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 585aa49c-8ae9-4818-ac87-253ddbbf1ce8 61 fields · synced Jul 25, 2026
  • EUDAMED 48ca44f7-1597-4912-b746-907db47d081b 61 fields · synced May 19, 2026
  • FDA UDI 0264d3c3-b21b-4cd8-9139-5b5164022a3e 33 fields · synced May 29, 2026