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

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Organization name
UDI-DI code
Reference / catalog number

HE210 — Class I MDR by MEDICAL PRECISION…

MD Atlas
MEDICAL PRECISION IMPLANTS, S.A.

EUDAMED last updated this device on Apr 30, 2026

HE210

84357230cp15W

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDICAL PRECISION IMPLANTS, S.A.
UDI-DI code: 08437023869284
Reference / catalog number: HE210

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Manufacturer information

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

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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

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	Aug 2, 2021	Still on market
Türkiye	Aug 2, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08437023869284
Basic UDI-DI: 84357230cp15W
Reference / catalog number: HE210
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: SCANBODY HE Ø3.3/3.5 mm
Additional information URL: https://mpimplants.com/eifu/
Clinical sizes: Ø3.3/3.5 mm

EMDN nomenclature code(s)

Q010299PROSTHETIC DENTISTRY 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

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Expiration date
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Software identification