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ChecQPEG DCQP102

by Dentis Co., Ltd

Ref DCQP102Model DENTIS Implant Surgical Instrument System

ChecQPEG DCQP102 is a medical device (EU MDR Class I; FDA Class I; FDA product code EKX, Handpiece, Direct Drive, Ac-Powered; EMDN category dental implants - accessories) made by Dentis Co., Ltd, registered in EUDAMED on 27 May 2026 (Basic UDI-DI 88061691DENTIS-I7L) and listed in FDA GUDID since 31 Mar 2025 (UDI-DI 08800053092500), active as of 23 Oct 2026.

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

CE MDR

Valid until

No date given

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

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number88061691DENTIS-I7L Basic UDI-DI 08800053092500UDI-DIDate27 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08800053092500 UDI-DI Date31 Mar 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 88061691DENTIS-I7L registered 27 May 2026 Active
  • FDA GUDID UDI-DI 08800053092500 listed 31 Mar 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08800053092500
  2. Registered EUDAMED 88061691DENTIS-I7L

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
ChecQ PEG EUDAMED
ChecQPEG GUDID
Generic name
Dental implant stability resonance frequency analysis peg
Device name
DENTIS Implant Surgical Instrument System
Model / reference
DCQP102, DENTIS Implant Surgical Instrument System
Primary DI / UDI-DI
08800053092500
Basic UDI-DI
88061691DENTIS-I7L
FDA product code
EKX
EMDN code
P01020180 Dental implants - accessories
GMDN term
Dental implant stability resonance frequency analysis peg
Device class
Class I
Regulation number
872.4200
EU registration type
Standard device
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental implant stability resonance frequency analysis peg

Similar devices in this category

Other devices filed under DENTAL IMPLANTS - ACCESSORIES.

Other devices from Dentis Co., Ltd

See all devices from Dentis Co., Ltd →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)