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Organization name
UDI-DI code
Reference / catalog number

Zygomatic Implants screwdriver — Class I MDR by BIOLOGITECH SRL

MD Atlas
BIOLOGITECH SRL

EUDAMED last updated this device on May 20, 2026

Zygomatic Implants screwdriver

805951396A13JH

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BIOLOGITECH SRL
UDI-DI code: 08059513963793
Reference / catalog number: CSZ

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Manufacturer information

Organization name: BIOLOGITECH SRL
SRN: IT-MF-000024415
Manufacturer status: Active

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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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: Zygomatic Implants screwdriver
UDI-DI code: 08059513963793
Basic UDI-DI: 805951396A13JH
Reference / catalog number: CSZ
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: https://www.biologitech.it/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Q010299PROSTHETIC DENTISTRY DEVICES - 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

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