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

DRSH0500 — Class I MDR by MORSA Wachswarenfabrik…

MD Atlas
MORSA Wachswarenfabrik Sallinger GmbH

EUDAMED last updated this device on Apr 18, 2024

DRSH0500

++D991DW82435NG

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MORSA Wachswarenfabrik Sallinger GmbH
UDI-DI code: +D991DR5002Y
Reference / catalog number: DRSH0500

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: MORSA Wachswarenfabrik Sallinger GmbH
SRN: DE-MF-000028586
Manufacturer status: Active

Related devices

DMSH0608++D991DW82435NGOn the market DMSH0602++D991DW82435NGOn the market DMSH0611++D991DW82435NGOn the market DMSH0605++D991DW82435NGOn the market DMSH0613++D991DW82435NGOn 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: not provided
UDI-DI code: +D991DR5002Y
Basic UDI-DI: ++D991DW82435NG
Reference / catalog number: DRSH0500
Issuing entity: HIBCC

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 25
Additional product description: Die Dentalwachse werden zur Bissregistrierung und Bissnahme sowie zum Schutz der Schleimhaut eingesetzt.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q01020199DENTAL IMPRESSION MATERIALS - 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