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.

Sterile Hyaluronic Acid Intra-Articular… — 3 UDI-DI variants, MDR

MD Atlas
Phibio GmbH

Data from EUDAMED, last updated May 23, 2026

Sterile Hyaluronic Acid Intra-Articular Gel Implant

42509062IACS6

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Manufacturer: Phibio 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

Legacy certificates

Certificate number: 1TD-MDR-0076/10/2025
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: Notice Belgelendirme, Muayene ve Denetim Hizmetleri Anonim Şirketi (2764)
Validity: Feb 25, 2026 → Oct 1, 2028

Identity & classification

Basic UDI-DI: 42509062IACS6
Device name: Sterile Hyaluronic Acid Intra-Articular Gel Implant
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class III
Version date: Feb 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: Phibio GmbH
SRN: DE-MF-000045435
Country: Germany
Email: info@phibio.de
Phone: ‎+49 162 3468981

Variants by status

UDI-DI variants

3 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

basicUdiUlid01KJAD9MKQQ8SW2T54JTAN50RP

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

Ortholand Cross 2.5%04250906203425
ViscoPhi Cross 2.0%04250906200530
ViscoPhi Cross 2.5%04250906200547