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Organization name
UDI-DI code
Reference / catalog number

DELTA CONTROL 1 22G 25MM — Class IIa MDR by Delta Med SPA

MD Atlas
Delta Med SPA

EUDAMED last updated this device on Feb 11, 2026

DELTA CONTROL 1 22G 25MM

8032248361008T

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Delta Med SPA
UDI-DI code: 08032248361102
Reference / catalog number: 3428122

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View device family (Basic UDI)

Manufacturer information

Organization name: Delta Med SPA
SRN: IT-MF-000027962
Manufacturer status: Active

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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

5 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.
CW032
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: DELTA CONTROL 1 22G 25MM
UDI-DI code: 08032248361102
Basic UDI-DI: 8032248361008T
Reference / catalog number: 3428122
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Peripheral Intravenous (IV) Catheter, single-way, consisting of a stainless steel needle, latest-generation Polyurethane (PUR) catheter, equipped with three radiopaque lines along its entire length. Peripheral intravenous catheter for short-term peripheral venous access which, in combination with other medical devices, allows the administration of fluids. Needle with triple-bevel tip. Passive safety system, activated without requiring additional actions by the healthcare operator beyond normal clinical practice. Easy to activate and non-reactivable. Double protection: The internal safety clip completely covers the needle tip, reducing the risk of accidental needlestick injury; the safety shield fully encapsulates the sharp, reducing the risk of blood contact and mucocutaneous exposure. Fully transparent flashback chamber, designed to provide optimal visualization of blood return. The device is equipped with “Blood Control” technology, which delays blood leakage following needle withdrawal, allowing the clinician to manage subsequent steps without immediate blood exposure. DO NOT USE 26G IV CATHETERS FOR HIGH-PRESSURE TREATMENTS.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 22G

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

C0101010202PERIPHERAL I.V. CATHETERS, WITH SAFETY SYSTEMS, W/O INJECTION VALVES

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

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