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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

ANC1022 — Class IIa MDR by Newclip Technics SAS

MD Atlas
Newclip Technics SAS

EUDAMED last updated this device on Apr 29, 2026

ANC1022

3700569600479A

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Newclip Technics SAS
UDI-DI code: 03700569643652
Reference / catalog number: ANC1022

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View device family (Basic UDI)

Manufacturer information

Organization name: Newclip Technics SAS
SRN: FR-MF-000011809
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

FR22/00000038Supplemented
Quality management systemNotified body: 1639Expiry: Sep 13, 2027

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW007
EUDAMED did not publish a description for this code.
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	Sep 14, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03700569643652
Basic UDI-DI: 3700569600479A
Reference / catalog number: ANC1022
Issuing entity: GS1

Classification

Risk category: Class IIa
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.

P091399ORTHOPAEDIC IMPLANT INSTRUMENTS, SINGLE-USE - 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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