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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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Raspatorien — 70 UDI-DI variants, MDR (Aesculap AG)

MD Atlas
Aesculap AG

Data from EUDAMED, last updated May 23, 2026

Raspatorien

40392390000003932F

70 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: Aesculap AG

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 40392390000003932F
Device name: Raspatorien
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 8, 2025

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

70 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K71CSFC29CXCKN1Z0W75J1XD

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

Aesculap04038653148745
Aesculap04038653166183
Aesculap04038653045341
Aesculap04046964072352
Aesculap04038653166190
ERGOPERIO04046964556197
ERGOPERIO04046964540158
ERGOPERIO04046964540141
ERGOPERIO04046955082247
SQ.line®04046955287406
SQ.line®04046955282869
SQ.line®04046955282876
SQ.line®04046955286164
SQ.line®04046955286225
SQ.line®04046955286195
SQ.line®04046955286201
SQ.line®04046955282852
SQ.line®04046955287819
SQ.line®04046955286218
SQ.line®04046955286188

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