Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

MS0006 — Class III MDD by Ferrosan Medical…

MD Atlas
Ferrosan Medical Devices A/S

EUDAMED last updated this device on Apr 25, 2026

MS0006

B-25712123000766

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Ferrosan Medical Devices A/S
UDI-DI code: 25712123000766
Reference / catalog number: MS0006

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: Ferrosan Medical Devices A/S
SRN: DK-MF-000002856
Manufacturer status: Active

Related devices

MS0007B-25712123000773On the market MS0005B-25712123000759On the market MS0004B-25712123000742On the market MS0008B-25712123000780On the market MS0002B-25712123000735On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Market distribution

Primary placement in Denmark; available across 1 country total.

Country	On market since	Until
DenmarkPrimary placement	Dec 13, 1996	Still on market

Device identification

Trade name: not provided
UDI-DI code: 25712123000766
Basic UDI-DI: B-25712123000766
Reference / catalog number: MS0006
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: SPONGOSTAN™ Absorbable Haemostatic Gelatin Sponge is a sterile, water-insoluble, malleable, porcine gelatin absorbable sponge intended for haemostatic use by applying to a bleeding surface.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M040503GELATINE SPONGE HAEMOSTATIC DRESSINGS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification