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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

B10351 — IVDR Class A IVDR by DIAGAST

MD Atlas
DIAGAST

EUDAMED last updated this device on Apr 27, 2026

B10351

3661562ABROMELINEXXXXXXQS

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: DIAGAST
UDI-DI code: 23661562103519
Reference / catalog number: B10351

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Manufacturer information

Organization name: DIAGAST
SRN: FR-MF-000012310
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 23661562103519
Basic UDI-DI: 3661562ABROMELINEXXXXXXQS
Reference / catalog number: B10351
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic 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: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0103030307ENZYMES (E.G. BROMELIN / PAPAIN, ETC.)

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

698603661562ABROMELINEXXXXXXQSOn the market 690243661562ABROMELINEXXXXXXQSOn the market 207003661562ACLEANSOLXXXXXXXKSOn the market 798513661562APLATESXXXXXXXXXUPOn the market 693013661562AEMTDILXXXXXXXXXH9On 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.