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

135516 — Class IIa MDD by Scheftner GmbH

MD Atlas
Scheftner GmbH

EUDAMED last updated this device on Apr 21, 2026

135516

B-04260207850730

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Scheftner GmbH
UDI-DI code: 04260207850730
Reference / catalog number: 135516

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: Scheftner GmbH
SRN: DE-MF-000049419
Manufacturer status: Active

Related devices

132717B-04260580284238On the market 132716B-04260207853137On the market 132165B-04260207853120On the market 132166B-04260580298532On the market 138118B-04260207851959On the market

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Oct 22, 2013	Jan 1, 2060

Device identification

Trade name: not provided
UDI-DI code: 04260207850730
Basic UDI-DI: B-04260207850730
Reference / catalog number: 135516
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Fräsrohling aus Reintitan Ti (Grade 4, mit Absatz) zur Herstellung von Zahnersatz.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q010601DENTAL ALLOYS

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

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.