FDA.reportPublic FDA data

Fine Micro Cannula

Primary DI
28809407786465
Brand
Fine Micro Cannula
Company
Feeltech Co.,Ltd.
Model
FTMN22-70-21
Catalog number
Fine Micro Cannula 22Gx70mm
Published
2019-09-22
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
FMINeedle, Hypodermic, Single Lumen

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FMINeedle, Hypodermic, Single LumenGeneral Hospital2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K092831000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K092831000DISPOSABLE HYPODERMIC NEEDLEFeel Tech2010-01-14FMI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
28809407786465PackageGS11200In Commercial Distribution
18809407786468PrimaryGS10
08809407786461Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
2880940778646528809407786465
1880940778646818809407786468
08809407786461088094077864618809407786461

GMDN Terms#

Term, Definition table
TermDefinition
Hypodermic needle, single-useA non-dedicated, sharp bevel-edged, hollow tubular device intended to be inserted beneath the skin of a patient while connected to a noninvasive device (e.g., syringe, secondary medication set) to administer and/or withdraw (aspirate) fluids/drugs; it may also be used for fluid/drug preparation. Some types are designed with a shielding mechanism (e.g., safety cap) for protection from sharp injuries. It is not specifically designed for blood collection or artery puncture, and does not have wings for fixation/placement (i.e., not a blood collection, intra-arterial, or venous butterfly needle). This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
688432407
Device count
24
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
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
18800145524299Miracu FCL LSCO 19Gx45mm3LS19V41003GA2026-08-25
18800145525913JBP V Line Edge 19Gx45mm3LS19V41003GA2026-08-25
18800145525920JBP V Line Force 19Gx70mm3BE19071621G2026-08-25
08800145524667JBP Nanocannula 23Gx40mmFTMN23-402026-04-16
18800145520697V-Soft Line BARB STAR 21Gx60mm FDA2160-101GD2026-03-19
18800145520932V-Soft Line BARB BLUNT CANNULA 23Gx60mm FDAF-FTN2363G2026-03-19
18800145521137V-Soft Line BARB BLUNT CANNULA L 21Gx60mm FDAL-FTN2162G2026-03-19
18800145521175V-Soft Line BARB BLUNT CANNULA L 21Gx90mm FDAL-FTN2192G2026-03-19
18800145521854V-Soft Line BARB BLUNT CANNULA L 19Gx40mm FDALC-FTN1942G2026-03-19
18800145522134V-Soft Line ARTE2 18Gx100mm FDA4PS118191603G2026-03-19
18800145522813V-Soft Line MONO 27Gx50mm FDA27055B2026-03-19
18800145523094V-Soft Line MONO 29Gx50mm FDA29056B2026-03-19
18800145523377V-Soft Line SCREW 27Gx50mm FDAS27055B2026-03-19
28800145520694V-Soft Line BARB STAR 21Gx60mm FDA2160-101GD2026-03-19
28800145520939V-Soft Line BARB BLUNT CANNULA 23Gx60mm FDAF-FTN2363G2026-03-19
28800145521134V-Soft Line BARB BLUNT CANNULA L 21Gx60mm FDAL-FTN2162G2026-03-19
28800145521172V-Soft Line BARB BLUNT CANNULA L 21Gx90mm FDAL-FTN2192G2026-03-19
28800145521851V-Soft Line BARB BLUNT CANNULA L 19Gx40mm FDALC-FTN1942G2026-03-19
28800145522131V-Soft Line ARTE2 18Gx100mm FDA4PS118191603G2026-03-19
28800145522810V-Soft Line MONO 27Gx50mm FDA27055B2026-03-19

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