Identity
- Trade Name
- SemiCut FDA UDI
- Generic Name
- End-cut biopsy gun handpiece/needle FDA UDI
- Device Name
- DISPOSABLE SEMIAUTOMATIC GUILLOTINE NEEDLE 16G X 100 mm FOR SOFT TISSUE BIOPSY WITHOUT REMOVABLE LUER FDA UDI
- Model / Reference
- PD01610 FDA UDI
- Description
- DISPOSABLE SEMIAUTOMATIC GUILLOTINE NEEDLE 16G X 100 mm FOR SOFT TISSUE BIOPSY WITHOUT REMOVABLE LUER FDA UDI
Identifiers
- Catalog Number
- PD01610 FDA UDI
- Primary DI / UDI-DI
- 08056138584990 FDA UDI
- 510(k) Number
- K160316 FDA UDI
- FDA Product Code
- FCG FDA UDIKNW FDA UDI
- GMDN Term
- End-cut biopsy gun handpiece/needle FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1075 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Dimensions & Sizes
- Size
- Needle Gauge — 16 Gauge FDA UDILength — 100 Millimeter FDA UDI
Category: End-cut biopsy gun handpiece/needle
SemiCut by M.d.l. S.r.l. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as End-cut biopsy gun handpiece/needle.
- Medline — MEDLINE INDUSTRIES, INC. · Class I
- Tru-Core™ II Biopsy Instrument — Argon Medical Devices, Inc. · Class II
- SuperCore™ Biopsy Instrument — Argon Medical Devices, Inc. · Class II
- Tru-Core™ II Biopsy Instrument — Argon Medical Devices, Inc. · Class II
- SuperCore Advantage™ — Argon Medical Devices, Inc. · Class II
- SuperCore Advantage™ — Argon Medical Devices, Inc. · Class II
- SuperCore™ Biopsy Instrument — Argon Medical Devices, Inc. · Class II
- SuperCore Advantage™ — Argon Medical Devices, Inc. · Class II
Cleared under the same submission
K160316 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- M.d.l. S.r.l.
Sources (1)
- FDA UDI a394c40a-0b49-4ccf-afb5-b1e5e9cc3f06 36 fields · synced Jun 8, 2026