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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

LHC-01 — Class I MDR by Telic, S.A.U.

MD Atlas
Telic, S.A.U.

EUDAMED last updated this device on May 15, 2026

LHC-01

8427734SURGLIGHTCOVER8F

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Telic, S.A.U.
UDI-DI code: 08427734013472
Reference / catalog number: LHC-01

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Manufacturer information

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

Critical warnings

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

CW022
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW020
EUDAMED did not publish a description for this code.

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: 08427734013472
Basic UDI-DI: 8427734SURGLIGHTCOVER8F
Reference / catalog number: LHC-01
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: Surgical light handle covers are a medical device intended to prevent medical staff intentionally or accidentally touching the handle of the light during a surgical procedure. The special toothed configuration of the inner plastic disk makes this device adaptable to any handle with diameter between 20 mm and 40 mm. Different lengths are available compatible with different handle measurements.
Additional information URL: https://www.telic.group/es/mub75
Clinical sizes: 95 MU50
120 MU50

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

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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.