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Gracey 1/2 SD DTS

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 201-202SDESTModel Dental hand instrument, curette for the removal of the supragingival calculus

by LM-Instruments Oy

Identity

Trade Name
Gracey 1/2 SD DTS EUDAMED
LMDental FDA UDI
Generic Name
Periodontal curette FDA UDI
Device Name
Periodontal hand instrument EUDAMED
Gracey 1/2 SD DTS, Curette, Periodontics FDA UDI
Model / Reference
201-202SDEST EUDAMEDFDA UDI
Dental hand instrument, curette for the removal of the supragingival calculus EUDAMED
Description
Gracey 1/2 SD DTS, Curette, Periodontics FDA UDI

Identifiers

Primary DI / UDI-DI
06438311205830 EUDAMEDFDA UDI
Basic UDI-DI
6438311PERIO1r06S EUDAMED
B-06438311205830 EUDAMED
Direct Marketing DI
06438311205830 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 1/2 SD DTS 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

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Manufacturer

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

Sources (3)

  • EUDAMED 9b41d362-4bd6-4776-8e54-24809491b271 61 fields · synced Sep 17, 2026
  • EUDAMED 99984328-7288-4359-9e75-2c390fe2056b 61 fields · synced May 17, 2026
  • FDA UDI cec4ae14-5576-4e1d-abba-dbbbc81f406e 33 fields · synced May 30, 2026