AMG

Primary DI
00810069260341
Brand
AMG
Company
ARROW MEDSOURCE GROUP LIMITED
Model
6001
Published
2021-03-09
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
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
K193526000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K193526000Syringe with safety needle, Safety needleJiangsu Caina Medical Co.,Ltd2020-07-17FMF

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10810069260348PackageGS1100In Commercial Distribution
20810069260345PackageGS112In Commercial Distribution
00810069260341PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1081006926034810810069260348
2081006926034520810069260345
00810069260341008100692603418100692603410810069260341

GMDN Terms#

Term, Definition table
TermDefinition
General-purpose syringe, single-useA sterile device consisting of a calibrated barrel (cylinder) with plunger intended to be used for injection/withdrawal of fluids/gas (e.g., medication) to/from a medical device or the body (i.e., capable of both); a needle is not included. It is intended for various medical applications and is not dedicated to medication administration. At the distal end of the barrel is a male connector (typically Luer-lock/slip type) for the attachment to a hypodermic needle or an administration set. It is typically made of plastic and silicone materials and may have anti-stick plunger allowing smooth plunger movement, either manually or by a syringe pump. This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
686378503
Device count
1
Lot or batch
true
Expiration date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00810069260327AMG9500-N952021-01-27
00850017650305AMGBCPB001XL2020-06-22
00850017650343AMGBCRW001XL2020-06-22
00850017650671AMGSCP00012020-08-06
00810069260358AMG60022021-03-08
00810069260365AMG60032021-03-09
00810069260372AMG60112021-03-09
00810069260389AMG60122021-03-09
00810069260396AMG60132021-03-09
00810069260402AMG20112021-05-14
00810069260419AMG20122021-05-14
00810069260426AMG20132021-05-14
00810069260433AMG20142021-05-14
00810069260440AMG20152021-05-14
00810069260457AMG20162021-05-14
10810069260409AMG20112021-05-14
10810069260416AMG20122021-05-14
10810069260423AMG20132021-05-14
10810069260430AMG20142021-05-14
10810069260447AMG20152021-05-14

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