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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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Dental Impression Copings — 38 UDI-DI variants, MDR

MD Atlas
GMI Dental Implantology, S.L.

Data from EUDAMED, last updated May 23, 2026

Dental Impression Copings

843656274KDS00FL

38 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: GMI Dental Implantology, S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843656274KDS00FL
Device name: Dental Impression Copings
Device model: 843656274KDS00FL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: GMI Dental Implantology, S.L.
SRN: ES-MF-000024246
Country: Spain
Email: info@gmidental.com
Phone: +34 973 18 43 50

Variants by status

UDI-DI variants

38 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS7VS7Y16BRBA6RGGHJ1TPYH

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

KDS0F361008436562747923
KDS0F000208436562743239
KDS0F361208436562748111
KDS0F400108436562743420
KDS0F400308436562743444
KDS0F001008436562743291
KDS0F400508436562748753
KDS0F400708436610700238
KDS0F000608436562743253
KDS0F001208436562743314
KDS0F360108436562743369
KDS0F001708436562745844
KDS0F400208436562743437

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