← Back to catalogue

Crane Kaplan

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 322-323ESModel Dental hand instrument, sickle scaler for the removal of the supragingival calculus

by LM-Instruments Oy

Identity

Trade Name
Crane Kaplan EUDAMED
LMDental FDA UDI
Generic Name
Manual dental scaler, reusable FDA UDI
Device Name
Periodontal hand instrument EUDAMED
Crane Kaplan, Scaler, Periodontics FDA UDI
Model / Reference
322-323ES EUDAMEDFDA UDI
Dental hand instrument, sickle scaler for the removal of the supragingival calculus EUDAMED
Description
Crane Kaplan, Scaler, Periodontics FDA UDI

Identifiers

Primary DI / UDI-DI
06438311213118 EUDAMEDFDA UDI
Basic UDI-DI
6438311PERIO1r06S EUDAMED
B-06438311213118 EUDAMED
Direct Marketing DI
06438311213118 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

Crane Kaplan 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

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 e856d3f2-eb52-414c-9458-ba29d7da740c 61 fields · synced Jul 17, 2026
  • EUDAMED 650f433c-7dda-496c-b754-2f6f6c25b20a 61 fields · synced May 19, 2026
  • FDA UDI 9c882f37-2a65-49d2-83f5-b1c76df34258 33 fields · synced May 30, 2026