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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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BENDA ELASTICA — 2 UDI-DI variants, MDR (Bericah S.p.A.)

MD Atlas
Bericah S.p.A.

Data from EUDAMED, last updated May 31, 2026

BENDA ELASTICA

8024151BENELN9

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: Bericah S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8024151BENELN9
Device name: BENDA ELASTICA
Device model: BENDA ELASTICA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 13, 2025

Manufacturer & authorised representative

Manufacturer

Name: Bericah S.p.A.
SRN: IT-MF-000007397
Country: Italy
Email: qualita@bericah.it
Phone: +390444240522

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K7EB3RFXW5J6FXM6Z58CCTA7

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

BENELA1DP08024151816848
BENELAFR1DP08024151818040