Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners 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

DT2-0840-70 — Class IIb MDR by DELPHOS IMPLANTS –…

MD Atlas
DELPHOS IMPLANTS – Indústria, Comércio, Importação e Exportação de Implantes Médicos, S.A.

EUDAMED last updated this device on Mar 12, 2026

DT2-0840-70

56004617PLMV3

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DELPHOS IMPLANTS – Indústria, Comércio, Importação e Exportação de Implantes Médicos, S.A.
UDI-DI code: 05600461703516
Reference / catalog number: DT2-0840-70

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?

View device family (Basic UDI)

Manufacturer information

Organization name: DELPHOS IMPLANTS – Indústria, Comércio, Importação e Exportação de Implantes Médicos, S.A.
SRN: PT-MF-000012964
Manufacturer status: Active

Related devices

Asymmetric Star Silver Plate 2.0mm - Left - bridge 00mm - thick.: 0.8mm56004617PLMV3On the market Asymmetric Star Silver Plate 2.0mm - Left - bridge 03mm - thick.: 0.8mm56004617PLMV3On the market Asymmetric Star Silver Plate 2.0mm - Left - bridge 05mm - thick.: 0.8mm56004617PLMV3On the market Asymmetric Star Silver Plate 2.0mm - Left - bridge 07mm - thick.: 0.8mm56004617PLMV3On the market Asymmetric Star Silver Plate 2.0mm - Left - bridge 09mm - thick.: 0.8mm56004617PLMV3On 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.

Critical warnings

5 warnings recorded — scroll inside the panel to see all entries.

CW029
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW136
EUDAMED did not publish a description for this code.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement	Jun 1, 2014	Still on market
Portugal	Jun 1, 2014	Still on market

Device identification

Trade name: not provided
UDI-DI code: 05600461703516
Basic UDI-DI: 56004617PLMV3
Reference / catalog number: DT2-0840-70
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: L Adjustment on Local Site Plate 2.0mm - Reversible - bridge 3mm - thick.: 0.8mm
Additional information URL: https://delphosimplants.com.pt/qualidade-regulamento-e-ifu/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05600461703516

Sign in to download the DataMatrix

Create a free account to download the UDI-DI DataMatrix for this device.

Email

Password

No account yet?

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

Sign in to generate the UDI-PI DataMatrix

Create a free account, then generate the compliant UDI-PI carrier for this device.

Email

Password

No account yet?

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

P09120503OSTEOSYNTHESIS SCREW-PLATE SYSTEMS

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

Become a partner of MD Atlas