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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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G3 — 7 UDI-DI variants, MDR (GRAPHITE MEDICAL)

MD Atlas
GRAPHITE MEDICAL

Data from EUDAMED, last updated May 19, 2026

G3

36156G32C

7 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: GRAPHITE MEDICAL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 36156G32C
Device name: G3
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 10, 2026

Manufacturer & authorised representative

Manufacturer

Name: GRAPHITE MEDICAL
SRN: FR-MF-000002504
Country: France
Email: info@graphite-medical.com

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KNVR3VFK0STW51P9M20X10E5

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

G3 6503615650000897
G3 5503615650000873
G3 7003615650000156
G3 5003615650000866
G3 6003615650000880
G3 4003615650000859
G3 3003615650000842