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.

Recording Paper (Z-fold, 210mm*140mm*14… — 1 UDI-DI variant, MDD

MD Atlas
S.I.D.EM. S.p.A.

Data from EUDAMED, last updated May 30, 2026

Recording Paper (Z-fold, 210mm140mm144P)

B-08050624190085

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: S.I.D.EM. S.p.A.

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

Measuring function

Legacy certificates

Certificate number: G2M0765960009
Type: refdata.legacy.mdd-certificate-type.v
Notified body: TÜV SÜD Product Service GmbH (0123)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-08050624190085
Device name: Recording Paper (Z-fold, 210mm*140mm*144P)
Device model: 01.57.471177-10
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: May 15, 2024

Manufacturer & authorised representative

Manufacturer

Name: S.I.D.EM. S.p.A.
SRN: IT-MF-000029977
Country: Italy
Email: lorenzo.om.banfi@sidemspa.it
Phone: +393518009161

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

basicUdiUlid01HXY48269BWRD14QVK4RQ9GME

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

01.57.471177-1008050624190085