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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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SurePal — 3 UDI-DI variants, MDR (AEROPHARM GmbH)

MD Atlas
AEROPHARM GmbH

Data from EUDAMED, last updated May 31, 2026

SurePal

7622436000001WK

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: AEROPHARM GmbH

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Device characteristics

Active deviceAdministers medicine

Identity & classification

Basic UDI-DI: 7622436000001WK
Device name: SurePal
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: AEROPHARM GmbH
SRN: DE-MF-000039064
Country: Germany
Email: Service.aeropharm@sandoz.com
Phone: +49 3672 479 0

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KS7QQF07NAGDDHJWZ3PJGBJT

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

SurePal 1047622436000051
SurePal 1547622436000068
SurePal 547622436000044