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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

VE-022 OP — Class IIa MDR by Telic, S.A.U.

MD Atlas
Telic, S.A.U.

EUDAMED last updated this device on Jul 18, 2024

VE-022 OP

8427734VEINSTRIPPERSZP

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Telic, S.A.U.
UDI-DI code: 08427734010648
Reference / catalog number: VE-022 OP

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Manufacturer information

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

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

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 Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	Jan 30, 1997	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08427734010648
Basic UDI-DI: 8427734VEINSTRIPPERSZP
Reference / catalog number: VE-022 OP
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Vein strippers are a single-use, ethylene oxide sterile medical device intended for the surgical removal of varicose veins. This product is not intended for use in the central venous system. Different models are available that are compatible with the two most common stripping techniques: Invagination stripping
Additional information URL: https://www.telic.group/fr/catalog/product/view/id/18311/s/extractor-venas-ve-0/category/2/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

C0699CARDIOVASCULAR SURGERY INSTRUMENTS, SINGLE-USE - 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

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.