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

848411 — Class I MDR by Telic, S.A.U.

MD Atlas
Telic, S.A.U.

EUDAMED last updated this device on May 18, 2026

848411

8427734USGELSTERILEPZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Telic, S.A.U.
UDI-DI code: 08427734036525
Reference / catalog number: 848411

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: Telic, S.A.U.
SRN: ES-MF-000001853
Manufacturer status: Active

Related devices

VE-0228427734VEINSTRIPPERSZPOn the market 20180028427734USGEL8LOn the market 6831UK8427734USGEL8LOn the market 76508427734BITEBLOCKKWOn the market AL-408427734TIPCLEANERJHOn 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.

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

Device identification

Trade name: not provided
UDI-DI code: 08427734036525
Basic UDI-DI: 8427734USGELSTERILEPZ
Reference / catalog number: 848411
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: Gel for ultrasound diagnosis and therapy. In sterile, single-dose packages. Intended to be used on mucous membranes and in natural body orifices. Also can be used for patients where cross contamination is a concern such as: - Patients with immunodeficiency or on immunosuppressive therapy. - Neonates or critically ill pediatric patients. - Critically ill patients or patients in contact, airborne or droplet transmission-based precautions. Distributed by Diagramm Halbach GmbH & Co. KG.
Additional information URL: https://www.telic.group/mub29
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z11040185ULTRASOUND SCANNERS - CONSUMABLES

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