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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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Proctoscope — 3 UDI-DI variants, MDR (SAPI MED S.p.A.)

MD Atlas
SAPI MED S.p.A.

Data from EUDAMED, last updated May 31, 2026

Proctoscope

803363880RCTSCSTVX

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: SAPI MED S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803363880RCTSCSTVX
Device name: —
Device model: Proctoscope
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: SAPI MED S.p.A.
SRN: IT-MF-000023733
Country: Italy
Email: paola@sapimed.com
Phone: +390131348109

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KKKV6MBZH9WZA0C3WNP0V5EN

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

Proctoscope08033638803783
Proctoscope08033638802205
Proctoscope08033638800638