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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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Banan pude L — 61 UDI-DI variants, MDR (Cobi Rehab A/S)

MD Atlas
Cobi Rehab A/S

Data from EUDAMED, last updated May 31, 2026

Banan pude L

5740000100014N5

61 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: 5740000100014N5
Device name: Banan pude L
Device model: 0305-101-000
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 15, 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

61 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JA7GR459RGMR6ZX2TBJ8QP63

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

0305-6011-00005740000104791
0305-6016-00005740000104821
0305-6021-00005740000104852
0305-6031-00005740000104890
0305-6001-00005740000104760
0305-6041-00005740000104920
0305-201-00005740000104456
0305-211-00005740000104487
0305-231-00005740000104548
0305-221-00005740000104517
0305-151-00005740000104425

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