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EasyLock

FDA UDI

Class I (US FDA UDI)

by M.d.l. S.r.l.

Identity

Trade Name
EasyLock FDA UDI
Generic Name
Body aspiration needle, single-use FDA UDI
Device Name
DISPOSABLE MENGHINI MODIFIED NEEDLE FOR SOFT TISSUE ASPIRATED BIOPSY 18G X 150 mm FDA UDI
Model / Reference
PC1815 FDA UDI
Description
DISPOSABLE MENGHINI MODIFIED NEEDLE FOR SOFT TISSUE ASPIRATED BIOPSY 18G X 150 mm FDA UDI

Identifiers

Catalog Number
PC1815 FDA UDI
Primary DI / UDI-DI
08056138584938 FDA UDI
FDA Product Code
MJG FDA UDI
GMDN Term
Body aspiration needle, 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

Yes

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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 18 Gauge FDA UDI
Length — 150 Millimeter FDA UDI

Category: Body aspiration needle, single-use

EasyLock by M.d.l. S.r.l. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Body aspiration needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
M.d.l. S.r.l.

Sources (1)

  • FDA UDI de9d834d-661b-4887-ab6a-011d28f5ad00 35 fields · synced May 30, 2026