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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

Stretcher Loading System — Class I MDR by Visser B.V.

MD Atlas
Visser B.V.

EUDAMED last updated this device on Nov 5, 2024

Stretcher Loading System

87208924758207W16300048

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Visser B.V.
UDI-DI code: 08720892475800
Reference / catalog number: 207W163000.000.0

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View device family (Basic UDI)

Manufacturer information

Organization name: Visser B.V.
SRN: NL-MF-000042565
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
Read User Manual before Use.

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Market distribution

Primary placement in XI; available across 1 country total.

Placed on the market in XI; per-country availability dates not published.

Device identification

Trade name: Stretcher Loading System
UDI-DI code: 08720892475800
Basic UDI-DI: 87208924758207W16300048
Reference / catalog number: 207W163000.000.0
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 Stretcher Loading System is intended to assist in the retrieval and transportation of patients in the Boxer Ambulance.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08720892475800

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

V0805038001RIGID SUPPORTS FOR LIFTS (STRETCHERS)

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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Related devices

Drawer Medical Work Station87208924758207W1628405MOn the market

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.