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

GenPlus Trio 2.0% — Class III MDR by Phibio GmbH

MD Atlas
Phibio GmbH

EUDAMED last updated this device on Mar 4, 2026

GenPlus Trio 2.0%

42509062IALSQ

On the marketClass III

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Phibio GmbH
UDI-DI code: 04250906203395
Reference / catalog number: PHI202DE-GNPT

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: Phibio GmbH
SRN: DE-MF-000045435
Manufacturer status: Active

Related devices

Artro DC426035399LNRLOn the market Artro DC 2.2%42509062IALSQOn the market GenPlus 2.0%42509062IALSQOn the market GenPlus 3.0%42509062IALSQOn the market GenPlus Trio 3.0%42509062IALSQOn the market

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
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	Nov 1, 2025	Nov 1, 2029

Device identification

Trade name: GenPlus Trio 2.0%
UDI-DI code: 04250906203395
Basic UDI-DI: 42509062IALSQ
Reference / catalog number: PHI202DE-GNPT
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Sterile Viscoelastic Gel Implant
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

P900402RESORBABLE FILLING AND RECONSTRUCTION DEVICES

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

Certificates

Certificate health across this manufacturer's portfolio.

1TD-MDR-0076/10/2025Issued
Technical documentationNotified body: 2764Expiry: Oct 1, 2028
2QMS-MDR-0076/10/2025Issued
Quality management systemNotified body: 2764Expiry: Oct 1, 2028
1TD-MDR-0076/10/2025Withdrawn
Technical documentationNotified body: 2764Expiry: Oct 1, 2028
6QMS-MDR-0076/06/2025Issued
Quality management systemNotified body: 2764Expiry: Jun 11, 2030