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

Dip'n'Twist — Class I MDD by senetics healthcare…

MD Atlas
senetics healthcare group GmbH & Co. KG

EUDAMED last updated this device on Mar 10, 2022

Dip'n'Twist

B-852741963T5

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: senetics healthcare group GmbH & Co. KG
UDI-DI code: D-852741963T5
Reference / catalog number: 789132465

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: senetics healthcare group GmbH & Co. KG
SRN: DE-MF-000018051
Manufacturer status: Inactive

Market distribution

Primary placement in Germany; available across 3 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
France		Still on market
XI		Still on market

Device identification

Trade name: Dip'n'Twist
UDI-DI code: D-852741963T5
Basic UDI-DI: B-852741963T5
Reference / catalog number: 789132465
Issuing entity: EUDAMED

Classification

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

Device details

Quantity: 1
Additional product description: dies ist ein tolles reinigungsprodukt
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0899MEDICAL SUPPORT EQUIPMENT - 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

Related devices

This device is not currently linked to any other device.

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.