Pricing Sign in

Role
Country
Date of registration
Address

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.

Organization name
UDI-DI code
Reference / catalog number

101015 — Class III MDR by Enzymatica AB

MD Atlas
Enzymatica AB

EUDAMED last updated this device on Feb 25, 2025

101015

73400311CZMSJE

On the marketClass III

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Enzymatica AB
UDI-DI code: 07340031105132
Reference / catalog number: 101015

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?

View device family (Basic UDI)

Manufacturer information

Organization name: Enzymatica AB
SRN: SE-MF-000002254
Manufacturer status: Active

Related devices

ColdZyme73400311CZMSJEOn the market 10101073400311CZMSJEOn the market ColdZyme73400311CZMSJEOn the market 10111573400311CZMSJEOn the market 101010B-101010KEOn the market

Certificates

Certificate health across this manufacturer's portfolio.

EPT 0477.MDR.24/5405Issued
Technical documentationNotified body: 0477Expiry: Mar 6, 2029
EPT 0477.MDR.24/5406Issued
Quality management systemNotified body: 0477Expiry: Mar 6, 2029

Critical warnings

No critical warnings reported for this device.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Austria; available across 1 country total.

Country	On market since	Until
AustriaPrimary placement	Apr 1, 2025	Mar 6, 2029

Device identification

Trade name: not provided
UDI-DI code: 07340031105132
Basic UDI-DI: 73400311CZMSJE
Reference / catalog number: 101015
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Mundspray - Behandlung und Linderung von erkältungs- und grippeähnlichen Symtomen
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07340031105132

Sign in to download the DataMatrix

Create a free account to download the UDI-DI DataMatrix for this device.

Email

Password

No account yet?

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

Sign in to generate the UDI-PI DataMatrix

Create a free account, then generate the compliant UDI-PI carrier for this device.

Email

Password

No account yet?

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

V9017ORAL ADMINISTRATION PREPARATIONS NOT INCLUDED IN OTHER CLASSES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Become a partner of MD Atlas