← Back to catalogue

Meco

EUDAMED

Class IIb (EU MDR)

Ref AC121Model S71022

by Zhejiang Longterm Medical Technology Co., Ltd.

Identity

Trade Name
MECO EUDAMED
Device Name
Silicone foam dressing EUDAMED
Model / Reference
S71022 EUDAMED
AC121 EUDAMED

Identifiers

Primary DI / UDI-DI
06926365544956 EUDAMED
Basic UDI-DI
69263655200047W EUDAMED
EMDN Code
M04040701 SILICONE DRESSINGS, NON-COMBINED EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany 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

Meco by Zhejiang Longterm Medical Technology Co., Ltd. — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000001161
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 1e421350-d06f-4559-b14f-2d18dd598664 61 fields · synced Jul 10, 2026