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OP-Stretch 175 30-30

EUDAMED

Class I (EU MDR)

Ref 180.3030.030Model InsertsRef S180.3030.030

by Eurotape B.V.

Identity

Trade Name
OP-Stretch 175 30-30 EUDAMED
Device Name
Inserts EUDAMED
Model / Reference
Inserts EUDAMED
180.3030.030 EUDAMED
S180.3030.030 EUDAMED

Identifiers

Primary DI / UDI-DI
08719925902727 EUDAMED
08719925907364 EUDAMED
Basic UDI-DI
871992590100IE9 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED
Italy 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

Category: Device sterilization/disinfection container, reusable

OP-Stretch 175 30-30 by Eurotape B.V. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Eurotape B.V.
EUDAMED SRN
NL-MF-000001956

Sources (2)

  • EUDAMED 46a8137b-d614-4526-bfe3-3c9239355df3 61 fields · synced Jul 21, 2026
  • EUDAMED 32ae002f-c6c4-4eff-b478-b7f793fb69b1 61 fields · synced May 18, 2026