Skip to content

Gracey 7/8

by LM-Instruments Oy 2 variants

Ref 207-208ESModel Dental hand instrument, curette for the removal of the supragingival calculus

Active European Union. Also listed in GUDID (US).

CE MDR CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED Number6438311PERIO1r06S Basic UDI-DI 06438311207018UDI-DIDate13 Oct 2023RegisteredStatusActive
European UnionCE/MDR EUDAMED Number6438311PERIO1r06S Basic UDI-DI 06438311207018UDI-DIDate13 Oct 2023RegisteredStatusActive
United StatesGUDID listing GUDID Number06438311207018 UDI-DI Date31 Aug 2020ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD, CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Gracey 7/8 EUDAMED
LMDental GUDID
Generic Name
Periodontal curette
Device Name
Periodontal hand instrument
Model / Reference
207-208ES, Dental hand instrument, curette for the removal of the supragingival calculus
Primary DI / UDI-DI
06438311207018
Basic UDI-DI
6438311PERIO1r06S, B-06438311207018
Direct Marketing DI
06438311207018
FDA Product Code
DZN
EMDN Code
L159001 Dental and periodontal curettes, reusable
GMDN Term
Periodontal curette
Device Class
Class I
Regulation Number
872.4565
EU market of registration
Finland
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Manufacturer details

EUDAMED SRN
FI-MF-000006705

Other devices from LM-Instruments Oy

See all devices from LM-Instruments Oy →

Properties

  • Reusable
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (20)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No