Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

KYF0C6405 — Class IIa MDR by GMI Dental…

MD Atlas
GMI Dental Implantology, S.L.

EUDAMED last updated this device on May 22, 2026

KYF0C6405

843656274KYF00J6

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: GMI Dental Implantology, S.L.
UDI-DI code: 08436562749064
Reference / catalog number: KYF0C6405

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: GMI Dental Implantology, S.L.
SRN: ES-MF-000024246
Manufacturer status: Active

Related devices

KDI0F3602843656274KDI00E2On the market KDI0F4005843656274KDI00E2On the market KDI0F3604843656274KDI00E2On the market KDI0F3601843656274KDI00E2On the market KDI0F4004843656274KDI00E2On the market

Market distribution

Primary placement in Spain; available across 3 countries total.

Country	On market since	Until
SpainPrimary placement		Still on market
France		Still on market
Portugal		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08436562749064
Basic UDI-DI: 843656274KYF00J6
Reference / catalog number: KYF0C6405
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://www.gmidental.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q010399SURGICAL DENTAL DEVICES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.