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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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MIASPAS instrument IIa — 10 UDI-DI variants, MDR (Aesculap AG)

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

MIASPAS instrument IIa

40392390000016612Q

10 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: Aesculap AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40392390000016612Q
Device name: MIASPAS instrument IIa
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 13, 2025

Manufacturer & authorised representative

Manufacturer

Name: Aesculap AG
SRN: DE-MF-000005504
Country: Germany
Email: eudamed@bbraun.com

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01K7EEB538R8KHSSWW0KR2WBS9

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

MIASPAS04038653167142
MIASPAS04038653152162
MIASPAS04038653265718
MIASPAS04038653265695
MIASPAS04038653265725
MIASPAS04038653265701
MIASPAS04038653266296
MIASPAS04038653152186
MIASPAS MINI-TTA04038653143160
MIASPAS MINI-TTA04038653143153