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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

113102 — Class IIa MDR by BIRR Biosciences BV

MD Atlas
BIRR Biosciences BV

EUDAMED last updated this device on Mar 23, 2026

113102

87179737110YM

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BIRR Biosciences BV
UDI-DI code: 08717973714491
Reference / catalog number: 113102

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View device family (Basic UDI)

Manufacturer information

Organization name: BIRR Biosciences BV
SRN: NL-MF-000023194
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

BE25/00000073Supplemented
Quality management systemNotified body: 1639Expiry: Mar 21, 2030

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	Mar 21, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08717973714491
Basic UDI-DI: 87179737110YM
Reference / catalog number: 113102
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 5
Additional product description: Containers for preparation of biological material for assisted reproduction.
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)08717973714491

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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.

U080207CONTAINERS FOR PREPARATION OF BIOLOGICAL MATERIAL FOR ASSISTED REPRODUCTION

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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