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LM-LiftOut S3 DTS

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 812230TModel Hand instrument for tooth extraction

by LM-Instruments Oy

Identity

Trade Name
LM-LiftOut S3 DTS EUDAMED
LMDental FDA UDI
Generic Name
Dental elevator, tooth/root FDA UDI
Device Name
LM-LiftOut S3 DTS, Extraction FDA UDI
Model / Reference
Hand instrument for tooth extraction EUDAMED
812230T EUDAMEDFDA UDI
Description
LM-LiftOut S3 DTS, Extraction FDA UDI

Identifiers

Primary DI / UDI-DI
06438311227801 EUDAMEDFDA UDI
Basic UDI-DI
B-06438311227801 EUDAMED
FDA Product Code
EMJ FDA UDI
EMDN Code
L150301 DENTAL EXTRACTION TOOTH FORCEPS, REUSABLE EUDAMED
GMDN Term
Dental elevator, tooth/root 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

LM-LiftOut S3 DTS by LM-Instruments Oy — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

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 (2)

  • EUDAMED 778bc682-a548-483e-80a7-008b9ed24320 61 fields · synced Jul 24, 2026
  • FDA UDI c94bfe42-d74d-4b10-9337-e66f494e6cc5 33 fields · synced May 29, 2026