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HandCut

FDA UDI

Class I (US FDA UDI)

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

Identity

Trade Name
HandCut FDA UDI
Generic Name
Soft-tissue biopsy procedure kit, non-medicated FDA UDI
Device Name
10 CS-DISPOSABLE NEEDLE 14G x 114MM FOR SOFT TISSUE BIOPSY WITH MANUAL ACTION FDA UDI
Model / Reference
PM14114 FDA UDI
Description
10 CS-DISPOSABLE NEEDLE 14G x 114MM FOR SOFT TISSUE BIOPSY WITH MANUAL ACTION FDA UDI

Identifiers

Catalog Number
PM14114 FDA UDI
Primary DI / UDI-DI
08052440105700 FDA UDI
FDA Product Code
MJG FDA UDI
GMDN Term
Soft-tissue biopsy procedure kit, non-medicated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 14 Gauge FDA UDI

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

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 090bc9e1-4c3c-4583-883a-f5bc94d7bf35 36 fields · synced Jun 8, 2026