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

NT920 — Class I MDR by CIE CONCORDE IMPORT…

MD Atlas
CIE CONCORDE IMPORT EXPORT

EUDAMED last updated this device on Feb 5, 2026

NT920

37015843STRABISM7H

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CIE CONCORDE IMPORT EXPORT
UDI-DI code: 03701584309011
Reference / catalog number: NT920

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: CIE CONCORDE IMPORT EXPORT
SRN: FR-MF-000003576
Manufacturer status: Active

Related devices

N75037015843TONGRETWCOn the market MIC01137015843FCPSINTUBATION8XOn the market 343137015843MICROADSONZQOn the market N21437015843GOUGEJPOn the market N82037015843NASALFORCEPSMHOn 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.

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

Device identification

Trade name: not provided
UDI-DI code: 03701584309011
Basic UDI-DI: 37015843STRABISM7H
Reference / catalog number: NT920
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)

L01040506TENOTOMY AND STRABISM CORRECTION SCISSORS, REUSABLE

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