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

ZERAMEX® WB Digital Implant Replica — Class I MDR

MD Atlas
CeramTec Schweiz GmbH

EUDAMED last updated this device on Oct 11, 2022

ZERAMEX® WB Digital Implant Replica

764016139XB3YYYYK01IPET

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CeramTec Schweiz GmbH
UDI-DI code: 07640161393752
Reference / catalog number: WB37522

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: CeramTec Schweiz GmbH
SRN: CH-MF-000024169
Manufacturer status: Active

Related devices

CERALOG® PL Implant driver, ISO-shaft L 22.8 mm764016139XT3XXXXKL2APIFWOn the market CERALOG® PL Implant driver, ISO-shaft L 27.8 mm764016139XT3XXXXKL2APIFWOn the market CERALOG® PL Implant removal driver L 23.0 mm764016139XT3XXXXKL2APIFWOn the market CERALOG® PL Impression post closed tray Ø 3.8 mm L 7.8 mm764016139XB3YYYYK01IPETOn the market CERALOG® PL Impression post closed tray Ø 4.3 mm L 7.8 mm764016139XB3YYYYK01IPETOn 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.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: ZERAMEX® WB Digital Implant Replica
UDI-DI code: 07640161393752
Basic UDI-DI: 764016139XB3YYYYK01IPET
Reference / catalog number: WB37522
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: ZERAMEX® WB Digital Implant Replica
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q010207DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY

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