COX for BIO-FEATHER

Primary DI
08055002903899
Brand
COX for BIO-FEATHER
Company
MEDAX SRL UNIPERSONALE
Model
CB20160-00
Device description
Introducer coaxial needle
Published
2018-03-07
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Rx
true
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
KNWInstrument, Biopsy

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KNWInstrument, BiopsyGastroenterology, Urology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K142125000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K142125000New Medax Biopsy SystemsMedax Srl Unipersonale2015-12-22KNW

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
18055002903896PackageGS110In Commercial Distribution
08055002903899PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
1805500290389618055002903896
08055002903899080550029038998055002903899

GMDN Terms#

Term, Definition table
TermDefinition
Needle guide, single-useA rigid, non-powered device designed to direct a sharp needle (not included) into its proper course when performing a clinical and/or surgical procedure; the guide itself is not intended for percutaneous access (not a guide-catheter). Dedicated needle guides are available for different procedures such as urethral injections, image-guided (e.g., ultrasound, MRI) transrectal/transperineal prostate biopsy or ablation, endocavity IVF procedures, percutaneous punctures, nerve blocks, electromagnetic device tracking surgery, and stereotactic breast biopsies. Procedural supportive devices (e.g., ultrasound transducer cover/sheath, drape) may be included with the device. This is a single-use device.

Regulatory Flags#

DUNS number
440211428
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
08052283955661COX for MEDONECO18160-102019-10-02
08052283955678COX for MEDONECO20100-102019-10-02
08052283955692MEDONEMO20200-K02019-10-02
08052283955715MED-BXB08100-002020-07-07
08052283955722MED-BXB08150-002020-07-07
08052283955739MED-BXB11100-002020-07-07
08052283955746MED-BXB11150-002020-07-07
08052283955753MED-BXB13070-002020-07-07
08052283955760MED-BXB13100-002020-07-07
08052283955777MED-BXB13150-002020-07-07
08052283955845MED-LXL08100-0S2020-07-07
08052283955852MED-LXL08150-0S2020-07-08
08052283955869MED-LXL11100-0S2020-07-08
08052283955876MED-LXL11150-0S2020-07-08
08052283955883MED-LXL13070-0S2020-07-08
08052283955890MED-LXL13100-0S2020-07-08
08052283955906MED-LXL13150-0S2020-07-08
08052283955913MED-LXL08100-0P2020-07-08
08052283955920MED-LXL08150-0P2020-07-08
08052283955937MED-LXL11100-0P2020-07-08

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
08800025901151BEXCORE Breast Biopsy SystemMedicalPark CO.,LTD.KNW2026-06-01
08800025902059BEXCORE Breast Biopsy SystemMedicalPark CO.,LTD.KNW2026-06-01
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