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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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Silberkanülen — 99 UDI-DI variants, MDR

MD Atlas
Primed Halberstadt Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Silberkanülen

42502032PRI06758

99 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Primed Halberstadt Medizintechnik GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42502032PRI06758
Device name: —
Device model: Silberkanülen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Feb 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: Primed Halberstadt Medizintechnik GmbH
SRN: DE-MF-000004967
Country: Germany
Email: primed@primed-halberstadt.de
Phone: +4939416686

Variants by status

UDI-DI variants

99 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KGKW9V1BX3SNBX4EPEVAQY6Q

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

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20289004250203227971
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20087504250203212984
20090504250203227414
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20087604250203212991
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20089204250203227254
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20089304250203227278
20090804250203227476
20090904250203227490
20088304250203250177
20089804250203250184
20088404250203227094
20086904250203212922

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