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

AMBRE250 — Class I MDR by H & Z Distribution

MD Atlas
H & Z Distribution

EUDAMED last updated this device on May 13, 2026

AMBRE250

377004217LOUPES-PLAST62

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: H & Z Distribution
UDI-DI code: 03770042179237
Reference / catalog number: AMBRE250

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: H & Z Distribution
SRN: FR-MF-000053127
Manufacturer status: Active

Related devices

AMBRE100377004217LOUPES-PLAST62On the market AMBRE150377004217LOUPES-PLAST62On the market AMBRE200377004217LOUPES-PLAST62On the market AMBRE300377004217LOUPES-PLAST62On the market AMBRE350377004217LOUPES-PLAST62On 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 1 country total.

Country	On market since	Until
FrancePrimary placement	Jun 1, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03770042179237
Basic UDI-DI: 377004217LOUPES-PLAST62
Reference / catalog number: AMBRE250
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: 54 MU50
2.5 MU104

EMDN nomenclature code(s)

Q0210030102READY TO WEAR PLASTIC SPECTACLES WITH ORGANIC LENSES

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