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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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Stand Alone Screws — 369 UDI-DI variants, MDR (Newclip Technics SAS)

MD Atlas
Newclip Technics SAS

Data from EUDAMED, last updated May 19, 2026

Stand Alone Screws

37005696002794

369 UDI-DI variants

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

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

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UDI-DI variants

369 UDI-DI variants

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Applied filters

basicUdiUlid01KPBB2KH83DPWSE5KDJ3FJ9F7

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

H1.1GFT3.0L2603700569639822
H1.1GFT2.6L2003700569648497
H1.1GFT3.0L24-ST03700569639815
H1.1GFT3.0L2203700569639785
H1.1HFT3.0L20D03700569662974
H0.9IFT2.25L26-ST03700569610890
H1.1HFT3.0L2403700569618216
H0.7HFT1.7L08D03700569642419
H1.1HFT2.6L12-ST03700569617844
H1.1IFT2.6L26-ST03700569618544
H0.9IFT2.25L1403700569610760
H0.7HFT1.7L16D03700569642488
H0.9HFT2.25L32-ST_V403700569610210
H0.9HFT2.25L1803700569610067
H1.1HFT2.6L10D03700569662615
H1.1IFT3.0L14-ST03700569618643
H1.1HFT3.0L36-ST03700569618346
H1.1HFT3.0L24D03700569663018
H1.1HFT2.6L2003700569617912
H1.1IFT2.6L20-ST03700569618483
H0.9HFT2.25L20D03700569662479
H1.1GFT3.0L16-ST03700569639730
H1.1HFT2.6L3403700569618056
H0.7GFT1.7L16D03700569672577
H1.1HFT3.0L12D03700569662899

1 2 3 4 5

Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 37005696002794
Device name: Stand Alone Screws
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 16, 2026

Manufacturer & authorised representative

Manufacturer

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

Variants by status