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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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Sterilisation Packaging — 7 UDI-DI variants, MDR

MD Atlas
CB Healthcare Consulting GmbH

Data from EUDAMED, last updated May 23, 2026

Sterilisation Packaging

4062183335046M

7 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: CB Healthcare Consulting GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4062183335046M
Device name: Sterilisation Packaging
Device model: TF-335 (CT)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: CB Healthcare Consulting GmbH
SRN: DE-MF-000005902
Country: Germany
Email: CBRegulatory@henryschein.de

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KKHB25Z05D6KR5CXG0Q6AKHZ

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

CYBERTECH14062183012075
CYBERTECH14062183012099
CYBERTECH14062183012051
CYBERTECH14062183012068
CYBERTECH14062183012105
CYBERTECH14062183012112
CYBERTECH14062183012082