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Sterile CleanWIPE® Medium Tip Foam Swab

EUDAMED

Class I (EU MDR)

Ref MP1302ST-2000Model MP1302ST-12

by Foamtec International Co., Ltd.

Identity

Device Name
Sterile CleanWIPE® Medium Tip Foam Swab EUDAMED
Model / Reference
MP1302ST-12 EUDAMED
MP1302ST-2000 EUDAMED

Identifiers

Primary DI / UDI-DI
08859694200058 EUDAMED
Basic UDI-DI
88596942MP1302ST5R EUDAMED
EMDN Code
A1101 SAMPLE COLLECTION NEUTRAL SWABS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: General-purpose absorbent tip applicator/swab, single-use

Sterile CleanWIPE® Medium Tip Foam Swab by Foamtec International Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose absorbent tip applicator/swab, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
TH-MF-000017561
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED d3f72746-ba60-4ae3-84d4-1979987e9e69 61 fields · synced Jun 18, 2026