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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

PER360FL25BPAF — Class IIa MDD by Didactic

MD Atlas
Didactic

EUDAMED last updated this device on May 18, 2026

PER360FL25BPAF

B-03661809029394

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Didactic
UDI-DI code: 03661809029394
Reference / catalog number: PER360FL25BPAF

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Manufacturer information

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

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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: 03661809029394
Basic UDI-DI: B-03661809029394
Reference / catalog number: PER360FL25BPAF
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: 3-way IV Infusion set with small drip chamber and last tube 60 cm total length : 210 cm – packed in blister 1 unit then bag of 25 units then outer carton with 10 bags of 25 units
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A03010101INFUSION CONTROLLERS WITH OR W/O AIR INLET

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