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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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P-I Scan Body Ti — 3 UDI-DI variants, MDR (SIC invent Sweden AB)

MD Atlas
SIC invent Sweden AB

Data from EUDAMED, last updated May 31, 2026

P-I Scan Body Ti

735017392ScanBodyTiEP

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: SIC invent Sweden AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 735017392ScanBodyTiEP
Device name: P-I Scan Body Ti
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: SIC invent Sweden AB
SRN: SE-MF-000002493
Country: Sweden
Email: support@pibranemark.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KPNBD3A8XHYFHR85KK730X83

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

P-I Dental Implant Systems07350173928582
P-I Dental Implant Systems07350173928575
P-I Dental Implant Systems07350173928599