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

2500 DOBLE ETIQ — Class IIb MDR by Telic, S.A.U.

MD Atlas
Telic, S.A.U.

EUDAMED last updated this device on Apr 28, 2026

2500 DOBLE ETIQ

8427734ESUPLATES3L

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Telic, S.A.U.
UDI-DI code: 08427734026748
Reference / catalog number: 2500 DOBLE ETIQ

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.

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08427734026748
Basic UDI-DI: 8427734ESUPLATES3L
Reference / catalog number: 2500 DOBLE ETIQ
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Pre-gelled electrosurgical plate.
Additional information URL: https://chrome-extension//efaidnbmnnnibpcajpcglclefindmkaj/https://www.telic.group/es/gsoft_ui/index/index/file/MUB72_20240509.pdf/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

K02010202ELECTROSURGERY DUAL PATIENT PADS (NEUTRAL ELECTRODES), SINGLE-USE

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