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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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Trays — 11 UDI-DI variants, MDR (devemed GmbH)

MD Atlas
devemed GmbH

Data from EUDAMED, last updated May 23, 2026

Trays

4061644PG0701013L

11 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: devemed GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4061644PG0701013L
Device name: Trays
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: devemed GmbH
SRN: DE-MF-000005568
Country: Germany
Email: info@devemed.de
Phone: +49 7467 9491990

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KGHCHQG3R3W5HGMBNCH7K5T3

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

4410-9504061644069651
4400-5504061644069392
4903-00 FBC04061644063734
4410-1004061644069286
4410-7004061644069361
4400-1004061644069231
4410-3004061644069323
4410-5004061644069347
4410-1504061644069309
4400-1504061644069255
4400-5004061644069279