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Organization name
UDI-DI code
Reference / catalog number

I-LiNQ Impression Post peek — Class I MDR by Novodent SA

MD Atlas
Novodent SA

EUDAMED last updated this device on May 20, 2024

I-LiNQ Impression Post peek

764016818003D7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Novodent SA
UDI-DI code: 07630188204827
Reference / catalog number: I-SILIPpe

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Manufacturer information

Organization name: Novodent SA
SRN: CH-MF-000023309
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.

Market distribution

Primary placement in Türkiye; available across 1 country total.

Country	On market since	Until
TürkiyePrimary placement	Sep 28, 2023	Still on market

Device identification

Trade name: I-LiNQ Impression Post peek
UDI-DI code: 07630188204827
Basic UDI-DI: 764016818003D7
Reference / catalog number: I-SILIPpe
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: I-LiNQ Impression Post peek
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

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

UDI-PI traceability

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