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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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LINEA CAVIGLIA — 16 UDI-DI variants, MDR (PAVIS SPA)

MD Atlas
PAVIS SPA

Data from EUDAMED, last updated May 31, 2026

LINEA CAVIGLIA

80287180000070MU

16 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: PAVIS SPA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 80287180000070MU
Device name: LINEA CAVIGLIA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: PAVIS SPA
SRN: IT-MF-000018588
Country: Italy
Email: info@pavis.it
Phone: 0332455463

Variants by status

UDI-DI variants

16 UDI-DI variants

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Applied filters

basicUdiUlid01KRN864H2ECT9FVEKVMJKNK8X

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

015BLBY08028718150529
015BL TAGLIA UNICA08028718150505
016BL L08028718460529
016BL M08028718460512
016BL S08028718460505
016BL XL08028718460536
016BL XXL08028718460543
010BL - TAGLIA UNICA08028718100500
020BL EX08028718200514
020BL REG08028718200507
020BL SMALL(PEDIATRIC)08028718200521
017BL XL08028718250533
017BL L08028718250526
017BL M08028718250519
017BL S08028718250502
017BL XXL08028718250540