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

Cap 1 — Class I MDR by MDB TEXINOV

MD Atlas
MDB TEXINOV

EUDAMED last updated this device on Jan 13, 2026

Cap 1

3770021816TEXTILES66

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MDB TEXINOV
UDI-DI code: 03770021816030
Reference / catalog number: CAP 1

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: MDB TEXINOV
SRN: FR-MF-000001728
Manufacturer status: Active

Related devices

Texishield CH-A033770021816MASQUESHFOn the market Texishield CH-B013770021816MASQUESHFOn the market Cap 23770021816TEXTILES66On the market FLUXMED 1V13770021816FLUXMEDJ8On the market FLUXMED 1V23770021816FLUXMEDJ8On 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 France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement		Still on market
Germany		Still on market

Device identification

Trade name: Cap 1
UDI-DI code: 03770021816030
Basic UDI-DI: 3770021816TEXTILES66
Reference / catalog number: CAP 1
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: Bonnet CAP 1
Additional information URL: https://www.fluxmedicare.fr/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12040280GENERAL MEDICINE THERAPEUTIC TREATMENT INSTRUMENTS - HARDWARE ACCESSORIES

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