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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

INNNOBAG8L — Class I MDR by INNOVATION GROUP S.R.L.

MD Atlas
INNOVATION GROUP S.R.L.

EUDAMED last updated this device on Apr 29, 2026

INNNOBAG8L

805201122INNOVATIONBAGXB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: INNOVATION GROUP S.R.L.
UDI-DI code: 08052011220054
Reference / catalog number: INNNOBAG8L

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View device family (Basic UDI)

Manufacturer information

Organization name: INNOVATION GROUP S.R.L.
SRN: IT-MF-000044378
Manufacturer status: Active

Related devices

INNOBAG2L 805201122INNOVATIONBAGXBOn the market INNNOBAG2LS 805201122INNOVATIONBAGXBOn the market INNNOBAG5LS 805201122INNOVATIONBAGXBOn the market INNOBAG5C 805201122INNOVATIONBAGXBOn the market INNOBAG5L805201122INNOVATIONBAGXBOn 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

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08052011220054
Basic UDI-DI: 805201122INNOVATIONBAGXB
Reference / catalog number: INNNOBAG8L
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: 50
Additional product description: —
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)08052011220054

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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.

A06030301URINE COLLECTION BAGS

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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