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SteriStretch® 35-80

EUDAMED

Class I (EU MDR)

Ref 170.3535.080Model Inserts

by Eurotape B.V.

Identity

Trade Name
SteriStretch® 35-80 EUDAMED
Device Name
Inserts EUDAMED
Model / Reference
Inserts EUDAMED
170.3535.080 EUDAMED

Identifiers

Primary DI / UDI-DI
08719925905285 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

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

SteriStretch® 35-80 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 (1)

  • EUDAMED be22056e-d8c0-4c61-b453-2cbebdf60261 61 fields · synced Jun 19, 2026