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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

4700181K — Class I MDR by Transatlantic HG Stolpe…

MD Atlas
Transatlantic HG Stolpe & Co. mbH

EUDAMED last updated this device on Aug 6, 2024

4700181K

4050856UMBCT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Transatlantic HG Stolpe & Co. mbH
UDI-DI code: 04050856047274
Reference / catalog number: 4700181K

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Manufacturer information

Organization name: Transatlantic HG Stolpe & Co. mbH
SRN: DE-MF-000009432
Manufacturer status: Active

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.

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 04050856047274
Basic UDI-DI: 4050856UMBCT
Reference / catalog number: 4700181K
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 transfer sheet is an aid for transferring patients from one stretcher or bed to another (lifting, pushing or pulling). It also serves as an absorbent carpet pad for stretchers, stretchers and beds.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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