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

PV163045F3 — Class IIb MDD by FEG Textiltechnik…

MD Atlas
FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH

EUDAMED last updated this device on Apr 2, 2026

PV163045F3

B-04250274706139

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH
UDI-DI code: 04250274706139
Reference / catalog number: PV163045F3

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: FEG Textiltechnik Forschungs- und Entwicklungsgesellschaft mbH
SRN: DE-MF-000005284
Manufacturer status: Active

Related devices

PV091515F1B-04250274703268On the market PV121217F1B-04250274704869On the market IP082030F1B-04250274704395On the market PV162030F1B-04250274701998On the market PV781715F1B-04250274705590On the market

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Oct 18, 2011	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04250274706139
Basic UDI-DI: B-04250274706139
Reference / catalog number: PV163045F3
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

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

EMDN nomenclature code(s)

P900299SURGICAL MESHES - 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

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.