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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

BODIPACK+ — Class I MDR by STERLAB

MD Atlas
STERLAB

EUDAMED last updated this device on Apr 24, 2025

BODIPACK+

376031457BDR5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: STERLAB
UDI-DI code: 03760314570794
Reference / catalog number: 311

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Manufacturer information

Organization name: STERLAB
SRN: FR-MF-000001369
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: BODIPACK+
UDI-DI code: 03760314570794
Basic UDI-DI: 376031457BDR5
Reference / catalog number: 311
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: 120
Additional product description: BOWIE AND DICK TEST PACK
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

S9080DEVICES FOR STERILISATION (EXCLUDING CAT. D - Z) - ACCESSORIES

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

Related devices

AQUAVAP376031457AQUAVAPK7On the market AQUAVAP376031457AQUAVAPK7On the market AQUAVAP376031457AQUAVAPK7On the market BODIPACK+376031457BDR5On the market EUROTEST376031457BDR5On 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.