Publix Short Needle Insulin Syringe

Primary DI
10041415024783
Brand
Publix Short Needle Insulin Syringe
Company
PUBLIX SUPER MARKETS, INC.
Model
192164
Device description
Publix 1/2cc, 5/16 inch x 31 gauge insulin syringe, 100ct
Published
2016-09-23
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
FMFSyringe, Piston
FMINeedle, Hypodermic, Single Lumen

Product Code Classifications#

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

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K062702000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K062702000ULTICARE DISPOSABLE SYRINGES AND NEEDLESUltimed, Inc.2006-11-29FMF

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
20041415018789PackageGS110In Commercial Distribution
30041415018786PackageGS15In Commercial Distribution
10041415024783PrimaryGS10
00041415024786Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
2004141501878920041415018789
3004141501878630041415018786
1004141502478310041415024783
00041415024786000414150247860414150247860041415024786

GMDN Terms#

Term, Definition table
TermDefinition
Insulin syringe/needle, basicA sterile device consisting of a calibrated barrel (cylinder) with plunger intended to be used to administer an injection of insulin to a patient subcutaneously; a non-retractable needle is included, either attached or detached (usually capped for user protection). The syringe is typically made of plastic and silicone materials and will have plunger anti-sticking properties allowing smooth plunger movement. It can be used by healthcare personnel or patient, and will allow for the aspiration of the pharmaceutical from its container for direct administration to the patient or via an intravenous (IV) port, heparin lock, or saline lock. This is a single-use device.

Regulatory Flags#

DUNS number
006922009
Device count
10
Lot or batch
true
Expiration date on label
true
No natural rubber latex
true

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