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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

RES-01-3237 — Class I MDR by EnvisionTEC GmbH

MD Atlas
EnvisionTEC GmbH

EUDAMED last updated this device on Nov 19, 2021

RES-01-3237

426068322FLEXCERASMILEYJ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: EnvisionTEC GmbH
UDI-DI code: 04260683220553
Reference / catalog number: RES-01-3237

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Manufacturer information

Organization name: EnvisionTEC GmbH
SRN: DE-MF-000009311
Manufacturer status: Active

Related devices

RES-01-3213426068322EGUARD7WOn the market RES-01-3212426068322EGUIDE7WOn the market RES-01-3214426068322ETRAYA3On the market RES-01-3244426068322FLEXCERABASEL9On the market RES-01-3242426068322FLEXCERABASEL9On 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.

CW010
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: not provided
UDI-DI code: 04260683220553
Basic UDI-DI: 426068322FLEXCERASMILEYJ
Reference / catalog number: RES-01-3237
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)

Q010699MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification