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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

ACQUASTOP MGA — Class I MDR by TAUMEDIPLAST s.r.l.

MD Atlas
TAUMEDIPLAST s.r.l.

EUDAMED last updated this device on May 11, 2026

ACQUASTOP MGA

805635138021826

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: TAUMEDIPLAST s.r.l.
UDI-DI code: 08056351380218
Reference / catalog number: ACQUASTOP MGA

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View device family (Basic UDI)

Manufacturer information

Organization name: TAUMEDIPLAST s.r.l.
SRN: IT-MF-000031607
Manufacturer status: Active

Related devices

ACQUASTOP BIA805635138017125On the market ACQUASTOP BIP80563513801882NOn the market ACQUASTOP GIA805635138022523On the market ACQUASTOP MBA80563513801952KOn the market ACQUASTOP MBP8056351380201ZJOn 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.

CW022
If you cut it, it shall not work.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Jun 11, 2008	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08056351380218
Basic UDI-DI: 805635138021826
Reference / catalog number: ACQUASTOP MGA
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: Submersible, watertight and reusable cast and bandage cover, size: adult half leg
Additional information URL: https://www.taumediplast.com/product_view.asp?ID=1
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)08056351380218

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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.

Y090699DEVICES FOR BODY PROTECTION - 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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