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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

Ratchet Wrench — Class I MDR by Bio3 Implants GmbH

MD Atlas
Bio3 Implants GmbH

EUDAMED last updated this device on May 12, 2026

Ratchet Wrench

4060475BIO3DINWSVQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Bio3 Implants GmbH
UDI-DI code: 04060475002400
Reference / catalog number: HR

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Manufacturer information

Organization name: Bio3 Implants GmbH
SRN: DE-MF-000009538
Manufacturer status: Active

Related devices

Adaptor for Handpiece4060475BIO3DINHPU5On the market Adaptor for Ratchet4060475BIO3DINHPU5On the market Analog for Ball Attachment4060475BIO3DINLATKOn the market Analog for locators4060475BIO3DINLATKOn the market Analog Implant Laboratory for Aesthetic S4060475BIO3DINLATKOn 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

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

CW007
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: Ratchet Wrench
UDI-DI code: 04060475002400
Basic UDI-DI: 4060475BIO3DINWSVQ
Reference / catalog number: HR
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

P01020180DENTAL IMPLANTS - 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

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Expiration date
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Software identification