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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

855.0S — Class I MDR by KONG S.p.A.

MD Atlas
KONG S.p.A.

EUDAMED last updated this device on Sep 18, 2023

855.0S

8023577STRETCHERSQP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: KONG S.p.A.
UDI-DI code: 08023577044477
Reference / catalog number: 855.0S

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View device family (Basic UDI)

Manufacturer information

Organization name: KONG S.p.A.
SRN: IT-MF-000027905
Manufacturer status: Active

Related devices

880.078023577STRETCHERSQPOn the market 880.018023577STRETCHERSQPOn the market 880.068023577STRETCHERSQPOn the market 855.008023577STRETCHERSQPOn the market 855.0M8023577STRETCHERSQPOn 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.

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08023577044477
Basic UDI-DI: 8023577STRETCHERSQP
Reference / catalog number: 855.0S
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: Rescue bag
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

EMDN nomenclature code(s)

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

V08050199PATIENT TRANSFER STRETCHERS - OTHER

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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