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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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Dagrofil — 89 UDI-DI variants, MDR (B. Braun Surgical, S.A.)

MD Atlas
B. Braun Surgical, S.A.

Data from EUDAMED, last updated May 23, 2026

Dagrofil

40392390000005652L

89 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: B. Braun Surgical, S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40392390000005652L
Device name: Dagrofil
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: B. Braun Surgical, S.A.
SRN: ES-MF-000002083
Country: Spain
Email: eudamed@bbraun.com

Variants by status

UDI-DI variants

89 UDI-DI variants

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Applied filters

basicUdiUlid01K3TTWHZXS8S6SYC34HMX6CE8

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

No registered UDI-DI variants for this device family.