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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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Transepithelial abutment — 8 UDI-DI variants, MDR

MD Atlas
MEDICAL PRECISION IMPLANTS, S.A.

Data from EUDAMED, last updated May 23, 2026

Transepithelial abutment

84357230cp2bd4S

8 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: MEDICAL PRECISION IMPLANTS, S.A.

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 84357230cp2bd4S
Device name: —
Device model: Transepithelial abutment
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: MEDICAL PRECISION IMPLANTS, S.A.
SRN: ES-MF-000008091
Country: Spain
Email: r.bosch@mpimplants.com
Phone: +34916846063

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KMJ6NNWM5QPSZWYQ9RGQFMSE

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

CM56908435723003991
EXC77008435723003755
EXC76608435723003717
EXC76908435723003748
CM57108435723004011
CM57008435723004004
EXC76508435723003700
CM57208435723004028