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SuperCore™ Biopsy Instrument

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
SuperCore™ Biopsy Instrument FDA UDI
Generic Name
End-cut biopsy gun handpiece/needle FDA UDI
Device Name
SuperCore™ Biopsy Instrument 18ga x 20cm FDA UDI
Model / Reference
701118200 FDA UDI
Description
SuperCore™ Biopsy Instrument 18ga x 20cm FDA UDI

Identifiers

Catalog Number
701118200 FDA UDI
Primary DI / UDI-DI
00886333005871 FDA UDI
FDA Product Code
KNW 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

Yes

FDA UDI

Category: End-cut biopsy gun handpiece/needle

SuperCore™ Biopsy Instrument by Argon Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as End-cut biopsy gun handpiece/needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1358283b-fb49-46fa-af79-d96e1dd191f5 36 fields · synced Jun 9, 2026