Picture of SYRINGE 1.0ML 28GA 1/2IN BLS 500 SUS CA

Sorry - this product is no longer available

SYRINGE 1.0ML 28GA 1/2IN BLS 500 SUS CA

Manufacturer : Becton, Dickinson and Company Inc

Brand : BD PrecisionGlide Syringes, 1mL 28G x 1/2 Blisterpack

MFG item # : 329420

Catalog # : 329420

FDA Product Code Name : FMF

GMDN Term Name : Insulin syringe/needle, basic

Package quantity : 5

Source	Chain of Custody	Credentialed	Rating	In Stock	Price	Quantity	Exp.	Lead times	Min. Quantity	Quantity Increment

Product classification

Product classification:

Syringe, piston

Product code:

FMF

GTIN:

true

GMDN

Code:

Insulin syringe/needle, basic

Description:

A 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.

DEVICE

Single Use:

Otc:

Rx:

Device distribution status:

In Commercial Distribution

Device count:

100

Device kit:

Lot batch:

Expiration date:

STERILIZATION METHOD TYPES

Additional information

DEVICE SIZES

Device sizes type:

Length

Device size (Unit):

Millimeter

Device size (Value):

ENVIRONMENTAL CONDITIONS

Storage handling type:

Storage Environment Temperature

Storage handling high (Unit):

Degrees Celsius

Storage handling high (Value):

Storage handling low (Unit):

Degrees Celsius

Storage handling low (Value):

IDENTIFIERS

Device Id:

50382903294201

Device type:

Package

DI number:

30382903294207

Package status:

In Commercial Distribution

Package type:

Case

Recall history

Recall Date:

Status:

Recall Number:

View FDA Recall:

Product Documents