BioPince Ultra Full Core Biopsy Instrument 360-1580-02

GUDID 20886333224023

BioPince™ Ultra Full Core Biopsy Instrument 18ga x 15cm (use with optional Co-Axial Needle: MCXS1815BP)

ARGON MEDICAL DEVICES, INC.

End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle End-cut biopsy gun handpiece/needle
Primary Device ID20886333224023
NIH Device Record Keya767a22c-84be-44fb-bea5-47ffa10d6fdc
Commercial Distribution StatusIn Commercial Distribution
Brand NameBioPince Ultra Full Core Biopsy Instrument
Version Model Number360-1580-02
Catalog Number360-1580-02
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
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com

Device Dimensions

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100886333224029 [Primary]
GS120886333224023 [Package]
Contains: 00886333224029
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 Number2
Public Version Date2019-07-12
Device Publish Date2019-04-16

On-Brand Devices [BioPince Ultra Full Core Biopsy Instrument]

20886333224054BioPince™ Ultra Full Core Biopsy Instrument with Co-Axial Introducer Needle (Biopsy Instrument
20886333224047BioPince™ Ultra Full Core Biopsy Instrument 18ga x 20cm (use with optional Co-Axial Needle: MC
20886333224030BioPince™ Ultra Full Core Biopsy Instrument with Co-Axial Introducer Needle (Biopsy Instrument
20886333224023BioPince™ Ultra Full Core Biopsy Instrument 18ga x 15cm (use with optional Co-Axial Needle: MC
20886333224016BioPince™ Ultra Full Core Biopsy Instrument with Co-Axial Introducer Needle (Biopsy Instrumen
20886333224009BioPince™ Ultra Full Core Biopsy Instrument 18ga x 10cm (use with optional Co-Axial Needle: MC

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