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LM-Activator 55LOW

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 94055L

by LM-Instruments Oy

Identity

Trade Name
LM-Activator 55LOW EUDAMED
LMDental FDA UDI
Generic Name
Orthodontic retainer FDA UDI
Device Name
Removable orthodontic appliance EUDAMED
LM-Activator 55LOW FDA UDI
Model / Reference
94055L EUDAMEDFDA UDI
Description
LM-Activator 55LOW FDA UDI

Identifiers

Primary DI / UDI-DI
06438311222400 EUDAMEDFDA UDI
Basic UDI-DI
6438311ROA10UU EUDAMED
FDA Product Code
KMY FDA UDI
EMDN Code
Q010499 ORTHODONTIC DEVICES - OTHER EUDAMED
GMDN Term
Orthodontic retainer FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.5525 FDA UDI
Market of Registration
Finland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

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

Yes

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

LM-Activator 55LOW by LM-Instruments Oy — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

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 (2)

  • EUDAMED 37e74e01-9c36-4129-8a4a-8d87b7e81542 61 fields · synced Jun 20, 2026
  • FDA UDI 0b82efe8-034e-454f-bcfe-a62c11a65901 33 fields · synced May 30, 2026