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FastCutP

FDA UDI

Class I (US FDA UDI)

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

Identity

Trade Name
FastCutP FDA UDI
Generic Name
End-cut biopsy gun needle FDA UDI
Device Name
DISPOSABLE NEEDLE FOR SOFT TISSUE BIOPSY 16G x 120 mm COMPATIBLE AUTOMATIC PROMAG 2.5 ® GUN FDA UDI
Model / Reference
MGP1612 FDA UDI
Description
DISPOSABLE NEEDLE FOR SOFT TISSUE BIOPSY 16G x 120 mm COMPATIBLE AUTOMATIC PROMAG 2.5 ® GUN FDA UDI

Identifiers

Catalog Number
MGP1612 FDA UDI
Primary DI / UDI-DI
08056138584716 FDA UDI
FDA Product Code
MJG FDA UDI
GMDN Term
End-cut biopsy gun needle 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
Length — 120 Millimeter FDA UDI
Needle Gauge — 16 Gauge FDA UDI

Category: End-cut biopsy gun needle

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

Similar devices

Also classified as End-cut biopsy gun needle.

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 255d6172-3df1-4875-8e9f-0e54cf6cc390 35 fields · synced Jun 8, 2026