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

GDG 5 — Class I MDR by MEDICAL PRECISION…

MD Atlas
MEDICAL PRECISION IMPLANTS, S.A.

EUDAMED last updated this device on Apr 27, 2026

GDG 5

84357230DIRYK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDICAL PRECISION IMPLANTS, S.A.
UDI-DI code: 08435723014560
Reference / catalog number: GDG 5

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: MEDICAL PRECISION IMPLANTS, S.A.
SRN: ES-MF-000008091
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW007
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 2 countries total.

Country	On market since	Until
SpainPrimary placement	May 5, 2022	Still on market
Türkiye	May 5, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08435723014560
Basic UDI-DI: 84357230DIRYK
Reference / catalog number: GDG 5
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: INSTRUMENTO DENTAL PARALELIZADOR DE IMPLANTE Ø 5 mm
Additional information URL: https://mpimplants.com/ifus/
Clinical sizes: Ø 5 mm

EMDN nomenclature code(s)

Q0199ODONTOLOGY 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

Related devices

IECM413084357230iecmP5On the market PDC 4084357230PDS3On the market IECM3713084357230iecmP5On the market IECM3710084357230iecmP5On the market BLOC-EX84357230sop183On the market

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.