← Back to catalogue

Her-Spec™

EUDAMED

Class I (EU MDR)

Ref C020520Model C020100-1

by CooperSurgical, Inc.

Identity

Trade Name
HER-SPEC™ EUDAMED
Device Name
ER SPEC Small, Non-Sterile EUDAMED
Model / Reference
C020100-1 EUDAMED
C020520 EUDAMED

Identifiers

Primary DI / UDI-DI
00888937027419 EUDAMED
Basic UDI-DI
0888937TD121ns2S EUDAMED
EMDN Code
U089006 VAGINAL SPECULUM, SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

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

Her-Spec™ by CooperSurgical, Inc. — Class I — 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
US-MF-000002607
Authorised Representative
CooperSurgical Distribution B.V. NL-AR-000000059

Sources (1)

  • EUDAMED 9d7c679f-ef2f-4d66-a3ce-db23eafd6d9b 61 fields · synced Jul 25, 2026