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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 20° — 13 UDI-DI variants, MDR (GRAPHITE MEDICAL)

MD Atlas
GRAPHITE MEDICAL

Data from EUDAMED, last updated May 19, 2026

G1 20°

36156G120S9

13 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: 36156G120S9
Device name: G1 20°
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

13 UDI-DI variants

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Applied filters

basicUdiUlid01KNRWMB7C6XP5E7QT98MNA7XF

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

G1 40 XS.2003615650000095
G1 60 L.2003615650003126
G1 60 XL.2003615650003133
G1 50 XXXL.2003615650000453
G1 50 S.2003615650000101
G1 60 M.2003615650003119
G1 50 L.2003615650000415
G1 40 S.2003615650000088
G1 30 XS.2003615650000071
G1 25 XXS.2003615650000064
G1 50 XL.2003615650000439
G1 50 M.2003615650000422
G1 50 XXL.2003615650000446