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.

Supposte di glicerolo — 4 UDI-DI variants, MDR

MD Atlas
Aeffe Farmaceutici S.r.l.

Data from EUDAMED, last updated May 31, 2026

Supposte di glicerolo

805259703DT0025T

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: Aeffe Farmaceutici 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

No device characteristics flagged

Legacy certificates

Certificate number: IT347304
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: BUREAU VERITAS ITALIA S.P.A. (1370)
Validity: Nov 17, 2025 → Nov 16, 2030

Identity & classification

Basic UDI-DI: 805259703DT0025T
Device name: —
Device model: Supposte di glicerolo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Feb 3, 2026

Manufacturer & authorised representative

Manufacturer

Name: Aeffe Farmaceutici S.r.l.
SRN: IT-MF-000028925
Country: Italy
Email: rvergnano@aeffefarma.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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

basicUdiUlid01KGHZZ3VHZY5Z9PF93GRVFMJW

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

PF_I0078720108052597030054
01908052597030368
PF_I0164020108052597030016
PF_I0130020108052597030009