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

FD-1072NS — Class I MDR by DMC Medical Ltd

MD Atlas
DMC Medical Ltd

EUDAMED last updated this device on Jan 22, 2026

FD-1072NS

5391530751FD-1072NS59

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DMC Medical Ltd
UDI-DI code: 05391530752718
Reference / catalog number: FD-1072NS

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: DMC Medical Ltd
SRN: IE-MF-000014755
Manufacturer status: Active

Related devices

FD-1131NS5391530751FD-1131NS4KOn the market FD-1051NS5391530751FD-1051NS4NOn the market FD-1029NS5391530751FD-1029NS59On the market FD-1055NS 5391530751FD-1055NS5AOn the market FD-1104NS5391530751FD-1104NS4DOn 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 Ireland; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 05391530752718
Basic UDI-DI: 5391530751FD-1072NS59
Reference / catalog number: FD-1072NS
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)

A02010602INSULIN SYRINGES W/O FIXED NEEDLES, 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