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Elesta - Introducer

FDA UDIEUDAMED

Class I (US FDA UDI)

by Elesta Spa

Identity

Trade Name
Elesta - Introducer FDA UDI
Generic Name
Interventional radiology percutaneous-access kit, single-use FDA UDI
Device Name
CHIBA Introducer needle, 21Gx20.6 cm FDA UDI
Model / Reference
CH2120. 6EC FDA UDI
Description
CHIBA Introducer needle, 21Gx20.6 cm FDA UDI

Identifiers

Primary DI / UDI-DI
08052286590012 FDA UDI
FDA Product Code
GAA FDA UDI
GMDN Term
Interventional radiology percutaneous-access kit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 21 Gauge FDA UDI
Length — 206 Millimeter FDA UDI

Category: Interventional radiology percutaneous-access kit, single-use

Elesta - Introducer by Elesta Spa — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Interventional radiology percutaneous-access kit, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elesta Spa

Sources (2)

  • FDA UDI ca660437-30db-49a3-8636-ffdc50f5aca5 34 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 1, 2026