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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

7211 — Class I MDR by Implants Diffusion…

MD Atlas
Implants Diffusion International

EUDAMED last updated this device on May 26, 2026

7211

03662174INSTRUL2

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Implants Diffusion International
UDI-DI code: 03662174003606
Reference / catalog number: 7211

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View device family (Basic UDI)

Manufacturer information

Organization name: Implants Diffusion International
SRN: FR-MF-000000597
Manufacturer status: Active

Related devices

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Certificates

Certificate health across this manufacturer's portfolio.

FR25/00000112Issued
Quality management systemNotified body: 1639Expiry: May 12, 2030

Critical warnings

No critical warnings reported for this device.

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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: 7211
UDI-DI code: 03662174003606
Basic UDI-DI: 03662174INSTRUL2
Reference / catalog number: 7211
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: Etroit rotationnel
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.

P01020180DENTAL IMPLANTS - ACCESSORIES

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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