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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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Xtend Connect Shape A200 — 2 UDI-DI variants, MDR (C LindheXtend AB)

MD Atlas
C LindheXtend AB

Data from EUDAMED, last updated May 31, 2026

Xtend Connect Shape A200

735010414A200UQ

2 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: C LindheXtend AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 735010414A200UQ
Device name: Xtend Connect Shape A200
Device model: A200
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: C LindheXtend AB
SRN: SE-MF-000005639
Country: Sweden
Email: info@lindhe.se
Phone: +46 35-262 92 00

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KS5EC16J8Q5ZNBZ18W9C43DD

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

Xtend Connect Shape A20007350104141028
Xtend Connect Shape A20007350104141011