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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

SlingCare Straight Up — Class I MDR by Indes Healthcare BV

MD Atlas
Indes Healthcare BV

EUDAMED last updated this device on Jun 14, 2022

SlingCare Straight Up

87202994521LINE3X

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Indes Healthcare BV
UDI-DI code: 08720299452152
Reference / catalog number: E1206-4021, E1206-4500

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View device family (Basic UDI)

Manufacturer information

Organization name: Indes Healthcare BV
SRN: NL-MF-000000051
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement		Still on market

Device identification

Trade name: SlingCare Straight Up
UDI-DI code: 08720299452152
Basic UDI-DI: 87202994521LINE3X
Reference / catalog number: E1206-4021, E1206-4500
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: The ‘Slingcare Straight up’ is a relabeled version of the esense Line+. The Slingcare Straigh up patient lift is a passive patient lift, aimed at use with patients with no remaining mobility functions. Max. patient weight 175 kg.
Additional information URL: https://esense-moves.com/nl/producten/line/%20%20%20%20http://www.slingcare.com/passieve-tilliften/
Clinical sizes: 0–175 MU29

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

V0805030102ELECTRIC MOBILE LIFTS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.