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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

TELEGRAPH EVO REMOVAL TOOL — Class I MDR by FOURNITURES…

MD Atlas
FOURNITURES HOSPITALIERES INDUSTRIE

EUDAMED last updated this device on May 27, 2026

TELEGRAPH EVO REMOVAL TOOL

3661489TELEVOCIRMM3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: FOURNITURES HOSPITALIERES INDUSTRIE
UDI-DI code: 03661489333507
Reference / catalog number: 233350

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Manufacturer information

Organization name: FOURNITURES HOSPITALIERES INDUSTRIE
SRN: FR-MF-000000819
Manufacturer status: Active

Related devices

ARROW PRIME COVER3661489PANIERCIAHOn the market ARROW PRIME GLENOID SET V23661489PANIERCIAHOn the market BEPOD TIC TAC TRAY PIP CAGE V23661489PANIERCIAHOn the market 45B SCREW MINI KIT TRAY3661489PANIERCIAHOn the market ALL AIMER ARTHROSCOPIC LEFT OFFSET H636614892415ALLCIRMP6On the market

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement	Nov 18, 2025	Still on market
Italy		Still on market

Device identification

Trade name: TELEGRAPH EVO REMOVAL TOOL
UDI-DI code: 03661489333507
Basic UDI-DI: 3661489TELEVOCIRMM3
Reference / catalog number: 233350
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

L0999ORTHOPAEDIC AND TRAUMATOLOGICAL 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

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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.