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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 Nakkepuf — 14 UDI-DI variants, MDR (Cobi Rehab A/S)

MD Atlas
Cobi Rehab A/S

Data from EUDAMED, last updated May 31, 2026

Dental Nakkepuf

5740000100016N9

14 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: Cobi Rehab A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5740000100016N9
Device name: Dental Nakkepuf
Device model: 0319-7001-000
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 3, 2024

Manufacturer & authorised representative

Manufacturer

Name: Cobi Rehab A/S
SRN: DK-MF-000001370
Country: Denmark
Email: cobi@cobi.dk
Phone: +4570252522

Variants by status

UDI-DI variants

14 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J98R8RJ98Y583PPTYR49Z546

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

0319-7621-00005740000106481
0319-7601-00005740000106443
0319-7421-00005740000106399
0319-7401-00005740000106375
0319-7501-00005740000106412
0319-7406-00005740000108683
0319-7301-00005740000106351
0319-7201-00005740000106313
0319-7211-00005740000106337
0319-7606-00005740000106474
0319-7001-00005740000106276
0319-7821-00005740000106542
0319-7101-00005740000106290
0319-7701-00005740000106511