Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Angimesh R2, Angimesh R2-1, Angimesh… — 1 UDI-DI variant, MDR

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

Data from EUDAMED, last updated May 30, 2026

Angimesh R2, Angimesh R2-1, Angimesh R2-9

3310971FT01HERPEL6

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.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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: 3310971FT01HERPEL6
Device name: Angimesh R2, Angimesh R2-1, Angimesh R2-9
Device model: Mesh for abdominal hernia surgery in polyester monofilament and multifilament
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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01H57BSYZ2MKDHNC8SCA3WN9WG

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

R2-15X1508033109710411