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Senta Pur L

EUDAMEDFDA UDI

Class I (EU MDR)

Ref K121 BEKA Dusch- und Badelifter und deren Zubehöre

by BEKA-Hospitec GmbH

Identity

Trade Name
SENTA PUR L EUDAMED
Senta Bathing Lift FDA UDI
Generic Name
Mobile patient lifting system, electrically-powered FDA UDI
Device Name
EVE! EUDAMED
Senta Bathing Lift FDA UDI
Model / Reference
K121 BEKA Dusch- und Badelifter und deren Zubehöre EUDAMED
920101008S FDA UDI
Description
Senta Bathing Lift FDA UDI

Identifiers

Primary DI / UDI-DI
04260735020094 EUDAMEDFDA UDI
04260735020032 EUDAMED
04260735020056 EUDAMED
04260735020100 EUDAMED
Basic UDI-DI
426068189121BP EUDAMED
Direct Marketing DI
04260735020094 EUDAMED
04260735020032 EUDAMED
04260735020056 EUDAMED
04260735020100 EUDAMED
FDA Product Code
FSA FDA UDI
EMDN Code
Y093312 SHOWER STRETCHERS EUDAMED
GMDN Term
Mobile patient lifting system, electrically-powered FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.5510 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bathing/changing table, mobile

Senta Pur L by BEKA Hospitec GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bathing/changing table, mobile.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
BEKA-Hospitec GmbH
EUDAMED SRN
DE-MF-000013895

Sources (5)

  • EUDAMED da8b07e7-458b-413b-933d-f5815061cd16 61 fields · synced Jul 27, 2026
  • EUDAMED 783fd672-b913-4db0-82f0-c0d2af41a251 61 fields · synced May 17, 2026
  • EUDAMED e14cc1bf-63ad-4390-b94c-10888525c38d 61 fields · synced May 19, 2026
  • EUDAMED 27e4e441-e3f8-43e7-bfba-f94e92249875 61 fields · synced May 19, 2026
  • FDA UDI 3a30c39b-9c8c-42e6-b72f-2d63d2dd7381 33 fields · synced May 30, 2026