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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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CSL — 12 UDI-DI variants, MDR (GRAPHITE MEDICAL)

MD Atlas
GRAPHITE MEDICAL

Data from EUDAMED, last updated May 19, 2026

CSL

36156CSLHH

12 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: 36156CSLHH
Device name: CSL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 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

12 UDI-DI variants

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Applied filters

basicUdiUlid01KK8ZY18SFE3TMS42R6K2A74W

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

CSL 21 XS03615650002341
CSL 26 L03615650002365
CSL 21 XL03615650002334
CSL 26 XXL03615650002419
CSL 21 S03615650002327
CSL 26 XL03615650002396
CSL 21 M03615650002310
CSL 26 S03615650002389
CSL 26 XS03615650002402
CSL 21 XXL03615650002358
CSL 26 M03615650002372
CSL 21 L03615650002303