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

Ligateur LigaConfort XL à usage… — Class I MDR

MD Atlas
Etablissements Albert Legrand

EUDAMED last updated this device on Jul 9, 2025

Ligateur LigaConfort XL à usage unique

3701603412631RF

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Etablissements Albert Legrand
UDI-DI code: 03701603401757
Reference / catalog number: 12.631/1

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: Etablissements Albert Legrand
SRN: FR-MF-000029888
Manufacturer status: Active

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: Ligateur LigaConfort XL à usage unique
UDI-DI code: 03701603401757
Basic UDI-DI: 3701603412631RF
Reference / catalog number: 12.631/1
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: Single-use XL LigaConfort ligator
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

G020401HAEMORRHOID LIGATURE SETS

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

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.

Related devices

Anuscope adulte à bord droit avec poignée à usage unique3701603412045QUOn the market Anuscope adulte à bord droit sans poignée à usage unique3701603412035QROn the market Anuscope adulte bord biseauté avec poignée à usage unique37016034AUP229ZOn the market Anuscope adulte bord biseauté sans poignée à usage unique37016034AUL229DOn the market Anuscope adulte long à bord droit avec poignée à usage unique3701603412045LFROn the market