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

Perifit Care+ — Class I MDR by X6 Innovations

MD Atlas
X6 Innovations

EUDAMED last updated this device on Feb 18, 2026

Perifit Care+

3770014642PER002V7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: X6 Innovations
UDI-DI code: 03770014642172
Reference / catalog number: PER002

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: X6 Innovations
SRN: FR-MF-000029894
Manufacturer status: Active

Critical warnings

4 warnings recorded — scroll inside the panel to see all entries.

CW275
Do not use Perifit Care+ if you are pregnant.
CW083
Although Perifit Care+ is made with medical grade silicone, in very rare cases some particularly sensitive users may experience allergic reaction.
CW272
Wash your hands and your Perifit Care+ before and after every use with warm, soapy water
CW262
Do not share Perifit Care+ with others. Even with proper cleaning, sharing the probe increases your risk of infection

Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement	Jan 24, 2023	Dec 31, 2029
Germany	Jun 13, 2022	Dec 31, 2029

Device identification

Trade name: Perifit Care+
UDI-DI code: 03770014642172
Basic UDI-DI: 3770014642PER002V7
Reference / catalog number: PER002
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

U070301PELVIC FLOOR REHABILITATION DEVICES, BIOFEEDBACK, SINGLE-USE

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

Related devices

Perifit Care3770014642PER001V5On the market Perifit Care3770014642PER001V5On 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.