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UDI Compass

Prontosan® acute Wound Gel

Certificate valid

Snapshot 2026-10-31 · Link to EUDAMED

UDI-DI 07612449144752Basic UDI-DI 40392390000009212L

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Class III · MDR · B. Braun Medical AG

Identification

Model
—
Issuing agency
GS1
Device status
active
Sterile
No
Implantable
No
Measuring function
No
Reusable surgical
No

Certificates

2247049CE01

EU quality management system · unknown

Notified body: DEKRA Certification B.V. (0344)

Valid from 2024-09-25 · Expiry 2028-10-01

Scope not stated in certificate data.

Certificate’s own scope text — not a compliance opinion from UDI Compass.

2247049TD05

EU technical documentation assessment · valid

Notified body: DEKRA Certification B.V. (0344)

Valid from 2024-09-25 · Expiry 2029-09-01

Scope not stated in certificate data.

Certificate’s own scope text — not a compliance opinion from UDI Compass.

Manufacturer

B. Braun Medical AG

SRN CH-MF-000017781

CH · Sempach

manufacturer

Authorised representative: B. Braun Melsungen AG (DE-AR-000000202)

Related UDI-DIs

NameUDI-DICertificate
Prontosan® acute Wound Gel07612449132209
Certificate valid

Snapshot 2026-10-31 · Link to EUDAMED

Prontosan® acute Wound Gel07612449130854
Certificate valid

Snapshot 2026-10-31 · Link to EUDAMED

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/prontosan-acute-wound-gel-4752 · UDI page: /udi/07612449144752

All devices from B. Braun Medical AG