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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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Pointer Cannula — 3 UDI-DI variants, MDR (Ab medica sas)

MD Atlas
Ab medica sas

Data from EUDAMED, last updated May 31, 2026

Pointer Cannula

376034693PCTOFZ

3 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: Ab medica sas

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 376034693PCTOFZ
Device name: —
Device model: Pointer Cannula
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: Ab medica sas
SRN: FR-MF-000000154
Country: France
Email: abmedica@abmedica.fr
Phone: +33 2 48 51 59 93

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KRXDT2HA216HMVM855YNFW64

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

Pointer Cannula03760346938715
Pointer Cannula03760346938739
Pointer Cannula03760346938722