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Sickle LM-Laplander DTS

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 148-149ESTModel Dental hand instrument, sickle scaler for the removal of the supragingival calculus

by LM-Instruments Oy

Identity

Trade Name
Sickle LM-Laplander DTS EUDAMED
LMDental FDA UDI
Generic Name
Manual dental scaler, reusable FDA UDI
Device Name
Periodontal hand instrument EUDAMED
Sickle LM-Laplander DTS, Scaler, Periodontics FDA UDI
Model / Reference
Dental hand instrument, sickle scaler for the removal of the supragingival calculus EUDAMED
148-149EST EUDAMEDFDA UDI
Description
Sickle LM-Laplander DTS, Scaler, Periodontics FDA UDI

Identifiers

Primary DI / UDI-DI
06438311011486 EUDAMEDFDA UDI
Basic UDI-DI
B-06438311011486 EUDAMED
6438311PERIO1r06S EUDAMED
Direct Marketing DI
06438311011486 EUDAMED
FDA Product Code
DZN FDA UDI
EMDN Code
L159001 DENTAL AND PERIODONTAL CURETTES, REUSABLE EUDAMED
GMDN Term
Manual dental scaler, 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

Sickle LM-Laplander DTS 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

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Manufacturer

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

Sources (3)

  • EUDAMED bcf3818f-3b5b-4284-bf96-5e03adc0bfcd 61 fields · synced Aug 2, 2026
  • EUDAMED 903df216-e43c-420a-88d8-5ea2de2cd4c5 61 fields · synced May 19, 2026
  • FDA UDI 2414780e-6465-4e26-88cd-1a3b852f47c9 33 fields · synced May 30, 2026