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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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Instruments IIa — 67 UDI-DI variants, MDR (Newclip Technics SAS)

MD Atlas
Newclip Technics SAS

Data from EUDAMED, last updated May 19, 2026

Instruments IIa

3700569600479A

67 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Newclip Technics SAS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3700569600479A
Device name: Instruments IIa
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Newclip Technics SAS
SRN: FR-MF-000011809
Country: France
Email: regulatory@newcliptechnics.com

Variants by status

UDI-DI variants

67 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQ73A3YAN0GGNYMC19MFRMHC

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

ANC97603700569641160
ANC118403700569658298
ANC19803700569617677
ANC99303700569653095
ANC83903700569605100
ANC99403700569653101
ANC97303700569610418
ANC133303700569660871
ANC47603700569617714
ANC177103700569677503
ANC65603700569619459
ANC19903700569617691
ANC60703700569622558
ANC96903700569639457
ANC65903700569623401
ANC113403700569656560
ANC104003700569645618

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