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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

MTO-MINION1 — Class I MDR by MEDTEOR GmbH

MD Atlas
MEDTEOR GmbH

EUDAMED last updated this device on Mar 10, 2022

MTO-MINION1

42517778SCANBODY4Z

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MEDTEOR GmbH
UDI-DI code: 04251777801215
Reference / catalog number: MTO-MINION1

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Manufacturer information

Organization name: MEDTEOR GmbH
SRN: DE-MF-000019576
Manufacturer status: Active

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: not provided
UDI-DI code: 04251777801215
Basic UDI-DI: 42517778SCANBODY4Z
Reference / catalog number: MTO-MINION1
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://ifu.medteor.com/
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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

D-MA35-C0G4-ASB-04251777800928On the market MTO-D2T5-60B-04251777801154On the market MTO-MINION542517778SCANBODY4ZOn the market D-MA35-C2G2-ASB-04251777800973On the market D-MA35-C1G4-ASB-04251777800959On 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.