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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

NPC PTO 4016i — Class IIb MDR by MEDICAL PRECISION…

MD Atlas
MEDICAL PRECISION IMPLANTS, S.A.

EUDAMED last updated this device on Apr 30, 2026

NPC PTO 4016i

84357230cp2bh52

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDICAL PRECISION IMPLANTS, S.A.
UDI-DI code: 08435723005476
Reference / catalog number: NPC PTO 4016i

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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

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

CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW027
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	Apr 8, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08435723005476
Basic UDI-DI: 84357230cp2bh52
Reference / catalog number: NPC PTO 4016i
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: DENTAL PROSTHETIC COMPONENT TI-BASE NON-ROTATORY Ø4 x 1.5 mm
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 1.5 mm
Ø4

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
Manufacturing date
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Software identification