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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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Bender — 11 UDI-DI variants, MDR

MD Atlas
Astrolabe - Fabricação de Implantes Médicos, Lda

Data from EUDAMED, last updated May 31, 2026

Bender

56004328111060999000001TP

11 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: Astrolabe - Fabricação de Implantes Médicos, Lda

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 56004328111060999000001TP
Device name: Bender
Device model: Bender
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: Astrolabe - Fabricação de Implantes Médicos, Lda
SRN: PT-MF-000016588
Country: Portugal
Email: info@astrolabe-medical.com
Phone: +351 219672298

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSFCTYTHARBZKYKCMB897VYB

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

09.13.00.1003505600432838834
09.13.01.0002505600432820914
09.13.00.0004505600432811257
09.13.00.0273505600432808578
09.13.00.1273505600432811264
09.13.00.2273505600432811271
09.13.00.3354505600432820907
09.13.00.3273505600432811288
09.13.00.2003505600432838841
09.13.00.1217205600432808585
09.13.01.0002005600432811295