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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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G1 SC — 10 UDI-DI variants, MDR (GRAPHITE MEDICAL)

MD Atlas
GRAPHITE MEDICAL

Data from EUDAMED, last updated May 19, 2026

G1 SC

36156G1SCWD

10 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: 36156G1SCWD
Device name: G1 SC
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 9, 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

10 UDI-DI variants

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Applied filters

basicUdiUlid01KNSAXC1GXKGH5TM3BQ2BMKXH

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

SC 40 S03615650003058
SC 50 XXL03615650001375
SC 40 XXL03615650001351
SC 40 M03615650003041
SC 50 M03615650003072
SC 60 L03615650003096
SC 50 L03615650003065
SC 50 XL03615650003089
SC 40 XL03615650001368
SC 40 L03615650000361