Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

VITA LUMEX ® AC — Class IIa MDR by VITA Zahnfabrik H.…

MD Atlas
VITA Zahnfabrik H. Rauter GmbH & Co. KG

EUDAMED last updated this device on Jul 4, 2024

VITA LUMEX ® AC

++J017BB2PQ

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: VITA Zahnfabrik H. Rauter GmbH & Co. KG
UDI-DI code: J017B53143120
Reference / catalog number: B5314312

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: VITA Zahnfabrik H. Rauter GmbH & Co. KG
SRN: DE-MF-000005906
Manufacturer status: Active

Related devices

CEREC MTL Zirconia++J017CC2PYOn the market CEREC MTL Zirconia++J017CC2PYOn the market CEREC MTL Zirconia++J017CC2PYOn the market CEREC MTL Zirconia++J017CC2PYOn the market CEREC MTL Zirconia++J017CC2PYOn 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.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Nov 15, 2019	Still on market

Device identification

Trade name: VITA LUMEX ® AC
UDI-DI code: J017B53143120
Basic UDI-DI: ++J017BB2PQ
Reference / catalog number: B5314312
Issuing entity: HIBCC

Classification

Risk category: Class IIa
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.vita-zahnfabrik.com/
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