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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

POS1040 — Class I MDR by Andanza International

MD Atlas
Andanza International

EUDAMED last updated this device on Feb 1, 2023

POS1040

4260322POS1040HT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Andanza International
UDI-DI code: 04260322414305
Reference / catalog number: POS1040

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Manufacturer information

Organization name: Andanza International
SRN: DE-MF-000014213
Manufacturer status: Inactive

Related devices

Andanza Eco Abdominal Size 14260322POS1001AFUOn the market HIPL10104260322HIPL1010EUOn the market POS20304260322POS2030HXOn the market POS20504260322POS2050J5On the market HIPL10304260322HIPL1030F2On the market

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: 04260322414305
Basic UDI-DI: 4260322POS1040HT
Reference / catalog number: POS1040
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: XXL-4XL

EMDN nomenclature code(s)

M030402010101ELASTIC SUPPORT BANDAGES, NON-ADHESIVE, EXTENSIBLE IN ONE DIRECTION, HIGH EXTENSIBILITY

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

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.