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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

6mm femoral offset guide — Class I MDR by SACIMEX

MD Atlas
SACIMEX

EUDAMED last updated this device on May 27, 2026

6mm femoral offset guide

3665946INS008XW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SACIMEX
UDI-DI code: 03665946000506
Reference / catalog number: 14 33 96

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View device family (Basic UDI)

Manufacturer information

Organization name: SACIMEX
SRN: FR-MF-000011190
Manufacturer status: Active

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5mm femoral offset guide3665946INS008XWOn the market Cap3665946INS011XKOn the market Depth indicator3665946INS009XYOn the market Drill guide3665946INS003XLOn the market DT4 wire pusher3665946INS007XUOn the market

Certificates

Certificate health across this manufacturer's portfolio.

2026 PR 0068Issued
Quality assuranceNotified body: 0318Expiry: Jan 13, 2031

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: 6mm femoral offset guide
UDI-DI code: 03665946000506
Basic UDI-DI: 3665946INS008XW
Reference / catalog number: 14 33 96
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: 6 MU50

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)03665946000506

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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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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