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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 DEPTH GAUGE — Class I MDR by FOURNITURES…

MD Atlas
FOURNITURES HOSPITALIERES INDUSTRIE

EUDAMED last updated this device on May 27, 2026

TELEGRAPH EVO DEPTH GAUGE

3661489TELEVOCIRMM3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: FOURNITURES HOSPITALIERES INDUSTRIE
UDI-DI code: 03661489708237
Reference / catalog number: 270823

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View device family (Basic UDI)

Manufacturer information

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

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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.

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 DEPTH GAUGE
UDI-DI code: 03661489708237
Basic UDI-DI: 3661489TELEVOCIRMM3
Reference / catalog number: 270823
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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