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Upside Down Peri Bottle

EUDAMED

Class I (EU MDR)

Ref 06979012310053Model SW-PB-Ⅰ 300,SW-PB-Ⅰ 360,SW-PB-Ⅰ 380,SW-PB-Ⅰ 400,SW-PB-Ⅰ 420,SW-PB-Ⅰ 450,SW-PB-Ⅰ 500,SW-PB-Ⅰ 650,SW-PB-Ⅱ 300,SW-PB-Ⅱ 360,SW-PB-Ⅱ 380,SW-PB-Ⅱ 400,SW-PB-Ⅱ 420,SW-PB-Ⅱ 450,SW-PB-Ⅱ 500,SW-PB-Ⅱ 650

by Jiangsu Senwo Medical Technology Co., LTD

Identity

Device Name
Upside Down Peri Bottle EUDAMED
Model / Reference
SW-PB-Ⅰ 300,SW-PB-Ⅰ 360,SW-PB-Ⅰ 380,SW-PB-Ⅰ 400,SW-PB-Ⅰ 420,SW-PB-Ⅰ 450,SW-PB-Ⅰ 500,SW-PB-Ⅰ 650,SW-PB-Ⅱ 300,SW-PB-Ⅱ 360,SW-PB-Ⅱ 380,SW-PB-Ⅱ 400,SW-PB-Ⅱ 420,SW-PB-Ⅱ 450,SW-PB-Ⅱ 500,SW-PB-Ⅱ 650 EUDAMED
06979012310053 EUDAMED

Identifiers

Primary DI / UDI-DI
06979012310053 EUDAMED
Basic UDI-DI
69790123100537Z EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain 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

Upside Down Peri Bottle by Jiangsu Senwo Medical Technology Co., LTD — 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

EUDAMED SRN
CN-MF-000048978
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (1)

  • EUDAMED db35ce94-d677-4a14-9d99-9e36a5f388be 61 fields · synced Jul 15, 2026