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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

TransferMan® 4m — Class I MDR by BIOZOL Diagnostica…

MD Atlas
BIOZOL Diagnostica Vertrieb GmbH

EUDAMED last updated this device on Jun 26, 2025

TransferMan® 4m

426245279TransferMan4mPW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BIOZOL Diagnostica Vertrieb GmbH
UDI-DI code: 04262452790007
Reference / catalog number: EPE-5191000015

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Manufacturer information

Organization name: BIOZOL Diagnostica Vertrieb GmbH
SRN: DE-MF-000043808
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW273
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: TransferMan® 4m
UDI-DI code: 04262452790007
Basic UDI-DI: 426245279TransferMan4mPW
Reference / catalog number: EPE-5191000015
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: The TransferMan® 4m has been designed and manufactured to assist in the positioning of micro tools (e.g., microcapillaries or micro glass pipettes) under the microscope during assisted reproductive technologies (ART) such as: intracytoplasmic sperm injection (ICSI), or the collection of genetic material for the purpose of genetic preimplantation testing (PGT). It is intended to be used together with a microinjector (e.g. CellTram® 4m Air/Oil).
Additional information URL: https://cmi.calibrescientific.com/en
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

U08020399DEVICES FOR MICROMANIPULATION OF BIOLOGICAL MATERIAL FOR ASSISTED REPRODUCTION - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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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.