BioPince™ Full Core Biopsy Instrument 360-1580-01

GUDID 20886333004359

BioPince™ Full Core Biopsy Instrument 18G x 15cm

ARGON MEDICAL DEVICES, INC.

End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle
Primary Device ID20886333004359
NIH Device Record Keydac9f525-9d2e-48f7-80d2-6ba7e31dc178
Commercial Distribution StatusIn Commercial Distribution
Brand NameBioPince™ Full Core Biopsy Instrument
Version Model Number360-1580-01
Catalog Number360-1580-01
Company DUNS140727624
Company NameARGON MEDICAL DEVICES, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep Dry and Away from Sunlight

Device Identifiers

Device Issuing AgencyDevice ID
GS100886333004355 [Primary]
GS120886333004359 [Package]
Contains: 00886333004355
Package: Box [5 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KNWInstrument, Biopsy

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-07-12
Device Publish Date2016-09-01

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Trademark Results [BioPince]

Mark Image

Registration | Serial
Company
Trademark
Application Date
BIOPINCE
BIOPINCE
76502092 2804645 Live/Registered
ARGON MEDICAL DEVICES, INC.
2003-03-21

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