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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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Combi Mesh Plus, Combi Mesh Plus Pro,… — 1 UDI-DI variant, MDR

MD Atlas
ANGIOLOGICA B.M. S.R.L.

Data from EUDAMED, last updated May 30, 2026

Combi Mesh Plus, Combi Mesh Plus Pro, Combi Mesh Plus Umbilical, Combi Mesh Plus 2F

3310971FT01HERPUM6

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class III

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Manufacturer: ANGIOLOGICA B.M. S.R.L.

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Device characteristics

Implantable

Legacy certificates

Certificate number: 024-00-01-MDR
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: ITALCERT SRL (0426)
Validity: Sep 29, 2025 → Jul 5, 2028

Certificate number: 025-00-00-MDR
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: ITALCERT SRL (0426)
Validity: Jul 6, 2023 → Jul 5, 2028

Identity & classification

Basic UDI-DI: 3310971FT01HERPUM6
Device name: Combi Mesh Plus, Combi Mesh Plus Pro, Combi Mesh Plus Umbilical, Combi Mesh Plus 2F
Device model: Surgical mesh for abdominal hernias in polypropylene monofilament coated with polyurethane
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Version date: Jul 14, 2023

Manufacturer & authorised representative

Manufacturer

Name: ANGIOLOGICA B.M. S.R.L.
SRN: IT-MF-000030846
Country: Italy
Email: info@angiologica.com
Phone: +39 0382556616

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01H57BYYA0Q4S54ZJMRCJ72WDG

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

BMP-A9-10X1508033109711609