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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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Rectal Gel — 4 UDI-DI variants, MDR (Nirial Pharma srl)

MD Atlas
Nirial Pharma srl

Data from EUDAMED, last updated May 31, 2026

Rectal Gel

805299063PROCTO001UW

4 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Nirial Pharma srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805299063PROCTO001UW
Device name: Rectal Gel
Device model: PR01
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: Nirial Pharma srl
SRN: IT-MF-000018760
Country: Italy
Email: info@nirialpharma.com
Phone: +39 0287285230

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KPRB17QZEE7XHTWSN3J9J15V

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

1941208052990631025
5771308052990632473
6190040208052990632220
6180201208052990630981