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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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CABESTRILLO LONETA VERDE TALLA S — 5 UDI-DI variants, MDR

MD Atlas
ALGRAN MANUFACTURA SANITARIA, S.L.

Data from EUDAMED, last updated May 23, 2026

CABESTRILLO LONETA VERDE TALLA S

8437013CBTLOUR

5 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: ALGRAN MANUFACTURA SANITARIA, S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8437013CBTLOUR
Device name: CABESTRILLO LONETA VERDE TALLA S
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 3, 2026

Manufacturer & authorised representative

Manufacturer

Name: ALGRAN MANUFACTURA SANITARIA, S.L.
SRN: ES-MF-000042506
Country: Spain
Email: algran.sl@gmail.com
Phone: +34 65 619 57 77

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KQPV0H7MGHJTVHHBMT29K2BC

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

Z1020XL08437013599177
Z1020L08437013599184
Z1020M08437013599191
Z1020S08437013599207
Z1020XS08437013599214