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

RACCORDS DE DIALYSE LG200 — Class IIa MDD by HEMODIA SAS

MD Atlas
HEMODIA SAS

EUDAMED last updated this device on Dec 27, 2024

RACCORDS DE DIALYSE LG200

B-03661379253342

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: HEMODIA SAS
UDI-DI code: 03661379253342
Reference / catalog number: 9350_A

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: HEMODIA SAS
SRN: FR-MF-000007191
Manufacturer status: Active

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.

Critical warnings

3 warnings recorded — scroll inside the panel to see all entries.

CW001
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW999
Ne pas utiliser sur les populations pédiatriques.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: RACCORDS DE DIALYSE LG200
UDI-DI code: 03661379253342
Basic UDI-DI: B-03661379253342
Reference / catalog number: 9350_A
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Les tubulures et accessoires de tubulures de la gamme dialyse sont des dispositifs médicaux utilisés pour le traitement des patients souffrant d’insuffisance rénale chronique terminale et bénéficiant d'une suppléance rénale : hémodialyse. Ce raccord connecte la fistule ou le cathéter du patient (2 points de ponction) à la ligne artérielle ou veineuse. La longueur supplémentaire apportée entre le patient et le générateur permet d’éviter les risques de plicatures de la tubulure.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

F0299DIALYSIS LINES - OTHER

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

DOUBLEFLO Day Tube Set3661379FAB020002AEFOn the market DOUBLEFLO OUTFLOW TUBE SET3661379FAB020002AEFOn the market DOUBLEFLO PATIENT TUBE SET3661379FAB020002AEFOn the market 4-way pedal for "ArthroVims pump"3661379FAB0400001E5On the market BOUCHON LLFE V1 PSB-03661379264065

On the market