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Gracey 17/18 Mini SD DTS

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 247-248MSDESTModel Dental hand instrument, curette for the removal of the supragingival calculus

by LM-Instruments Oy

Identity

Trade Name
Gracey 17/18 Mini SD DTS EUDAMED
LMDental FDA UDI
Generic Name
Periodontal curette FDA UDI
Device Name
Periodontal hand instrument EUDAMED
Gracey 17/18 Mini SD DTS, Curette, Periodontics FDA UDI
Model / Reference
Dental hand instrument, curette for the removal of the supragingival calculus EUDAMED
247-248MSDEST EUDAMEDFDA UDI
Description
Gracey 17/18 Mini SD DTS, Curette, Periodontics FDA UDI

Identifiers

Primary DI / UDI-DI
06438311013275 EUDAMEDFDA UDI
Basic UDI-DI
B-06438311013275 EUDAMED
6438311PERIO1r06S EUDAMED
Direct Marketing DI
06438311013275 EUDAMED
FDA Product Code
DZN FDA UDI
EMDN Code
L159001 DENTAL AND PERIODONTAL CURETTES, REUSABLE EUDAMED
GMDN Term
Periodontal curette 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

Gracey 17/18 Mini SD 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 a5852256-bd24-4832-b8e5-184330a65b87 61 fields · synced Jul 14, 2026
  • EUDAMED 81b4e3b0-f2d6-4e22-945f-7ebe566576d6 61 fields · synced May 19, 2026
  • FDA UDI cedd8637-70e2-4782-a7ca-e01c299b74b4 33 fields · synced May 27, 2026