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P Pod

EUDAMEDFDA 510(k)

Class I (EU MDR)

Ref SOS10062A/S

by Drive DeVilbiss Healthcare Limited

Identity

Device Name
P Pod EUDAMED
Model / Reference
SOS10062A/S EUDAMED

Identifiers

Primary DI / UDI-DI
05056126030426 EUDAMED
Basic UDI-DI
50561260PPOD4100KB EUDAMED
EMDN Code
Y180980 SEATING SYSTEMS / POSTURE SYSTEMS / SEATING AIDS - ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Northern Ireland 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

P Pod by Drive DeVilbiss Healthcare Limited — Class I — FDA_510K, MDR — listed in EUDAMED, FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
GB-MF-000012818
Authorised Representative
Advena Limited MT-AR-000000234

Sources (2)

  • EUDAMED 5f92a47c-72f1-4adc-b582-25625e8f19bc 61 fields · synced Jun 18, 2026
  • FDA 510(k) K133397 1 fields · synced May 18, 2026