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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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Microtip applicators — 16 UDI-DI variants, MDR

MD Atlas
CB Healthcare Consulting GmbH

Data from EUDAMED, last updated May 23, 2026

Microtip applicators

4062183448037L

16 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: 4062183448037L
Device name: Microtip applicators
Device model: TF-448 (DEHP)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 16, 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

16 UDI-DI variants

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Applied filters

basicUdiUlid01KKVS849Q7866ZAXWY4R7TC5F

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

DEHP14062183028526
DEHP14062183026942
DEHP14062183028496
DEHP14062183028472
DEHP14062183028519
DEHP14062183026980
DEHP14062183027000
DEHP14062183028533
DEHP14062183028489
DEHP14062183026973
DEHP14062183028540
DEHP14062183026997
DEHP14062183026959
DEHP14062183026966
DEHP14062183028465
DEHP14062183028502