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

93422125 — Class I MDR by biocon Medizintechnik…

MD Atlas
biocon Medizintechnik GmbH

EUDAMED last updated this device on May 19, 2026

93422125

42514803001K7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: biocon Medizintechnik GmbH
UDI-DI code: 04251480301804
Reference / catalog number: 93422125

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: biocon Medizintechnik GmbH
SRN: DE-MF-000006429
Manufacturer status: Active

Critical warnings

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

CW001
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW007
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: 04251480301804
Basic UDI-DI: 42514803001K7
Reference / catalog number: 93422125
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: Kundenindividuell angefertigtes Einweg-Patientenabdecktuch oder -system, das für einen speziellen Eingriff im OP benötigt wird, steril.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 140 MU10
160 MU10

EMDN nomenclature code(s)

T020199SURGICAL DRAPES - 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

52598-00442514803047KXOn the market 52598-00142514803047KXOn the market 52598-00342514803047KXOn the market 9220012042514803001K7On the market 9342229942514803001K7On the market

Certificates

Certificate health across this manufacturer's portfolio.

44910200206Issued
Quality assuranceNotified body: 0044Expiry: Jan 25, 2031