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

BK 25 — Class I MDR by Dr. Jean Bausch GmbH &…

MD Atlas
Dr. Jean Bausch GmbH & Co. KG

EUDAMED last updated this device on Apr 2, 2026

BK 25

++E2102x0xFilmx8x12x16D5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Dr. Jean Bausch GmbH & Co. KG
UDI-DI code: +E210BK251B
Reference / catalog number: BK 25

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: Dr. Jean Bausch GmbH & Co. KG
SRN: DE-MF-000005577
Manufacturer status: Active

Related devices

BK 97++E2101x0xPaperx100x20085On the market BK 92++E2101x0xPaperx100x20085On the market BK 98++E2101x0xPaperx100x20085On the market BK 93++E2101x0xPaperx100x20085On the market BK 89++E2103x4xArtiBrux38On 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.

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.
CW032
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: +E210BK251B
Basic UDI-DI: ++E2102x0xFilmx8x12x16D5
Reference / catalog number: BK 25
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: 1
Additional product description: —
Additional information URL: https://www.bauschdental.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q01020299DENTAL CONTACT INDICATORS - 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