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

PBall-55 — Class I MDR by Febromed GmbH & Co. KG

MD Atlas
Febromed GmbH & Co. KG

EUDAMED last updated this device on Mar 6, 2024

PBall-55

426074055TRACAX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Febromed GmbH & Co. KG
UDI-DI code: 04260740550197
Reference / catalog number: PBall-55

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: Febromed GmbH & Co. KG
SRN: DE-MF-000009287
Manufacturer status: Active

Related devices

CP426074055TUBHCOn the market DGH - ALU426074055TRACAXOn the market DGH426074055TRACAXOn the market PBall-65426074055TRACAXOn the market CTRAC - 4000426074055TRACAXOn the market

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.

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04260740550197
Basic UDI-DI: 426074055TRACAX
Reference / catalog number: PBall-55
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: System: An dem, bei der Einleitung einer Geburt, Entspannungsübungen vorgenommen werden können.
Additional information URL: https://www.febromed.de/gebaersysteme/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V080299MEDICAL CHAIRS - OTHER
V0899MEDICAL SUPPORT EQUIPMENT - 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