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

PR3LVF50LFBPAF — Class IIa MDD by Didactic

MD Atlas
Didactic

EUDAMED last updated this device on May 18, 2026

PR3LVF50LFBPAF

B-03661809031472

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Didactic
UDI-DI code: 03661809031472
Reference / catalog number: PR3LVF50LFBPAF

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: Didactic
SRN: FR-MF-000000176
Manufacturer status: Active

Related devices

PMFML80FB-03661809030956On the market PR3LVM150LFBPAFB-03661809031076On the market BPCOVSTD3661809HELE5On the market GLNP9103661809LATEVOn the market B60012IC3661809HELE5On the market

Critical warnings

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

CW009
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW011
It is essential to check the tightness of the connections before use

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: not provided
UDI-DI code: 03661809031472
Basic UDI-DI: B-03661809031472
Reference / catalog number: PR3LVF50LFBPAF
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: Extension line with a 3-way stopcock that replace the a Luer Lock female of 1-way extension line
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A03020101LOW PRESSURE EXTENSION LINES

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

Certificate health across this manufacturer's portfolio.

ECM25MDR014Withdrawn
Quality management systemNotified body: 1282Expiry: Jul 28, 2030