Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners 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.

CALXYL® — 6 UDI-DI variants, MDR

MD Atlas
OCO-Präparate Herstellung und Vertrieb von pharmazeutischen Produkten GmbH

Data from EUDAMED, last updated May 23, 2026

CALXYL®

426074131-CALXYL-OCO-B9

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: OCO-Präparate Herstellung und Vertrieb von pharmazeutischen Produkten GmbH

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?

Device characteristics

Implantable

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 426074131-CALXYL-OCO-B9
Device name: CALXYL®
Device model: CALXYL® 20g
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 13, 2022

Manufacturer & authorised representative

Manufacturer

Name: OCO-Präparate Herstellung und Vertrieb von pharmazeutischen Produkten GmbH
SRN: DE-MF-000012362
Country: Germany
Email: info@oco-praeparate.de
Phone: +49 6238926810

Variants by status

UDI-DI variants

6 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01GK46177TYNYVZ8RAG22BYPJY

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

10001100 04260741310028
1000010004260741310004
1000410004260741310080
1000020004260741310011
1000120004260741310042
1000190004260741310097