Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ 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

WALLET — Class I MDR by HOPI MEDICAL

MD Atlas
HOPI MEDICAL

EUDAMED last updated this device on Oct 6, 2025

WALLET

3770034761WLMV02AJ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: HOPI MEDICAL
UDI-DI code: 37700347610446
Reference / catalog number: WALLET

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?

Manufacturer information

Organization name: HOPI MEDICAL
SRN: FR-MF-000038707
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: WALLET
UDI-DI code: 37700347610446
Basic UDI-DI: 3770034761WLMV02AJ
Reference / catalog number: WALLET
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Mobile station for teleconsultation with medical sensors, providing an integrated and portable healthcare solution.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12030692VITAL SIGNS TELEMETRY INSTRUMENTS - MEDICAL DEVICE SOFTWARE
V92MEDICAL DEVICE SOFTWARE - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

FMC3770034761FMCV03ZROn the market HOPACK3770034761HOPACKV01DCOn the market LIMSTAR3770034761LSTLJV0376On the market MINILIM3770034761MNLAMV02WKOn the market WALLIGHT3770034761WALLIGHT2GOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.