← Back to catalogue

neoheel

EUDAMED

Class IIa (EU MDR)

Ref 1050M

by Sterilance Medical (Suzhou) Inc.

Identity

Trade Name
neoheel EUDAMED
Device Name
Heel Incision EUDAMED
Model / Reference
1050M EUDAMED

Identifiers

Primary DI / UDI-DI
16945630116060 EUDAMED
Basic UDI-DI
6945630130BG EUDAMED
Unit of Use DI
06945630116063 EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

neoheel by Sterilance Medical (Suzhou) Inc. — Class IIa — 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-000002860
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED f873d5a3-dcde-4bc7-acc4-95f8f05b6b25 61 fields · synced May 29, 2026