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

I-CARE EZ-GO AMBULATORY 80 — Class I MDR by BMB MEDICAL

MD Atlas
BMB MEDICAL

EUDAMED last updated this device on Feb 8, 2024

I-CARE EZ-GO AMBULATORY 80

376034596EZVHAU7W2

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BMB MEDICAL
UDI-DI code: 37603459602128
Reference / catalog number: EZVHAU8

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: BMB MEDICAL
SRN: FR-MF-000011270
Manufacturer status: —

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: I-CARE EZ-GO AMBULATORY 80
UDI-DI code: 37603459602128
Basic UDI-DI: 376034596EZVHAU7W2
Reference / catalog number: EZVHAU8
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)

V08050103EMERGENCY AND TRAUMATOLOGY STRETCHERS

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

CARVI 60CM376034596CRCO6BSOn the market CARVI 70CM376034596CRCO6BSOn the market CARVI 80CM376034596CRCO6BSOn the market CLAVIA FCD 65376034596FCD7BDOn the market CLAVIA FCD 75376034596FCD7BDOn 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.