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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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Instrumentation class IIa — 20 UDI-DI variants, MDR

MD Atlas
Newclip Technics SAS

Data from EUDAMED, last updated May 19, 2026

Instrumentation class IIa

37005696004698

20 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

Reusable

Identity & classification

Basic UDI-DI: 37005696004698
Device name: Instrumentation class IIa
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 12, 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

20 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRDP0MXCZTMZDHE4ZSG35QQS

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

ANC18903700569620233
ANC28903700569621063
ANC29703700569621155
ANC31103700569621292
ANC18803700569620226
ANC29803700569621162
ANC311-ST03700569663223
ANC102603700569633714
ANC91803700569637309
ANC310-ST03700569663230
ANC1253-ST03700569678876
ANC54203700569622343
ANC29103700569621087
ANC61103700569622589
ANC125303700569657109
ANC18703700569620219
ANC31003700569621285
ANC28803700569621056
ANC19003700569620240
ANC29003700569621070