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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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Guided surgery sleeve — 4 UDI-DI variants, MDR

MD Atlas
Implants Diffusion International

Data from EUDAMED, last updated May 19, 2026

Guided surgery sleeve

03662174SURGSLEEVEJ4

4 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Implants Diffusion International

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 03662174SURGSLEEVEJ4
Device name: Guided surgery sleeve
Device model: Guided surgery sleeve
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 12, 2022

Manufacturer & authorised representative

Manufacturer

Name: Implants Diffusion International
SRN: FR-MF-000000597
Country: France
Email: rad@idi-dental.com
Phone: +33149707048

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01G0EKM4ZSKK1QDTJBBZZ8RD0T

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

D1503662174013797
D2003662174014497
D4203662174013773
D5203662174013780