SequaFilm

by Foshan United Medical Technologies Ltd. 2 variants

Ref SQ130607OModel many

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number693113223419B3 Basic UDI-DI 06931132220001UDI-DI	Date21 May 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Polyurethane film dressings
Model / Reference: many, SQ130607O

Primary DI / UDI-DI: 06931132220001
Basic UDI-DI: 693113223419B3
Direct Marketing DI: 06931132220001
EMDN Code: M04040601 Polyurethane dressings, non-combined

Device Class: Class I
EU market of registration: Spain

Manufacturer details

EUDAMED SRN: CN-MF-000017922
Authorised representative: Medwheat Tech Service GmbH DE-AR-000006844

Other devices from Foshan United Medical Technologies Ltd.

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Sorbsan Probe

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SequaFilm

Class I
Sequasorb Ag+

Class III
Sequa® Sorb 10x10cm

Class I
Sequa® Sorb 2.5x30cm

Class I

See all devices from Foshan United Medical Technologies Ltd. →

Properties

Sterile

Other properties (12)

Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No