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

IV402-52 — Class I MDR by Ivalmed S.L.

MD Atlas
Ivalmed S.L.

EUDAMED last updated this device on Apr 27, 2026

IV402-52

84357608INSGUIA5K

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Ivalmed S.L.
UDI-DI code: 08435760803691
Reference / catalog number: IV402-52

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: Ivalmed S.L.
SRN: ES-MF-000000634
Manufacturer status: Active

Related devices

IV780-5584357608ADAPTADORESRNOn the market IV780-9084357608ADAPTADORESRNOn the market IV784-77-0084357608ADAPTADORESRNOn the market IV784-78-0084357608ADAPTADORESRNOn the market IV784-10-0084357608ADAPTADORESRNOn 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.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	Apr 27, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08435760803691
Basic UDI-DI: 84357608INSGUIA5K
Reference / catalog number: IV402-52
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: Instrumento cuya funcion principal es guiar a otro instrumento donde se le requiere en el campo quirúrgico o fijar instrumentos de guia en su posicion correcta
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L0399GENERAL SURGERY INSTRUMENTS, REUSABLE - OTHER

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