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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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ProvEndo — 8 UDI-DI variants, MDR (Provepharm SAS)

MD Atlas
Provepharm SAS

Data from EUDAMED, last updated May 19, 2026

ProvEndo

376023716PVENDOGP

8 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Provepharm SAS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376023716PVENDOGP
Device name: ProvEndo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 25, 2024

Manufacturer & authorised representative

Manufacturer

Name: Provepharm SAS
SRN: FR-MF-000009343
Country: France
Email: contact@provepharm.com
Phone: +33491086930

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01HSTG84EY4X9139FMVYSW2W1J

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

00303760237160195
00303760237160331
00303760237160379
00303760237160317
00303760237160355
00303760237160393
00303760237160171
00303760237160416