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.

NOVOX PATCH — 4 UDI-DI variants, MDR (MOSS S.p.A.)

MD Atlas
MOSS S.p.A.

Data from EUDAMED, last updated May 30, 2026

NOVOX PATCH

805452935NPAM9

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: MOSS 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

No device characteristics flagged

Legacy certificates

Certificate number: EPT 0477.MDR.22/4952
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: Eurofins Product Testing Italy S.r.l. (0477)
Validity: Oct 7, 2022 → Oct 6, 2027

Identity & classification

Basic UDI-DI: 805452935NPAM9
Device name: NOVOX PATCH
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jan 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: MOSS S.p.A.
SRN: IT-MF-000010071
Country: Italy
Email: moss@moss-brand.it
Phone: +39 0322 772032

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

basicUdiUlid01KFGBHRJW9X1010T47Z4FA3DS

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

NPT2010-1-L208054529351749
NPT2010-1 08054529350735
NPT2010-10-L208054529351756
NPT2010-10 08054529350759