BD 309582 Syringe 3cc Luer Lok Tip ST DIS 25 Gauge 1 Inch 800/CS

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Description

BD 309582 Syringe 3cc Luer Lok Tip ST DIS 25 Gauge 1 Inch 800/CS

309582 – 3 mL BD Luer-Lok Syringe with attached needle 25 G x 1.5 in., Sterile, Single use

3cc, 25g x 1.5″, Standard Syringes with Needle

3mL Luer-Lok Syringe With 25G x 1.5″ PrecisionGlide Needle Combination. Regular bevel, regular wall. Detachable needle. World’s sharpest needle is combined with BD’s clear barrel featuring bold scale. Syringes have positive plunger rod stop and tapered plunger rod design.

BD conventional syringes are available with and without an attached needle. BD syringe-needle combinations feature a clear barrel with a bold scale. Disposable syringes with a BD Luer-Lok tip, luer slip tip or eccentric luer slip tip can be fitted with either a conventional needle or safety needle.

Key Product Features

Detachable Needle	Product has a Detachable Needle
Hub Color	Blue
Hub Material	Polypropylene
Hub Type	Luer
Needle Gauge	25 G
Needle Gauge (m)	0.50 mm
Needle Length (in.)	1.5 in.
Needle Length (m)	38.10 mm
Needle Tip Type	Regular
Needle Type	Hypodermic
Needle Wall Type	Regular
Priming Volume	0.086 mL
Pyrogen Free	Product is pyrogen free
Syringe Tip Orientation	Concentric
Syringe Tip Type	BD Luer-Lok
Syringe Scale	0.1 mL graduations
Total Shelf Life	1825
Sterile	Sterilized product
Volumetric Accuracy	+/- 5% *for 1ml or smaller,accuracy below 0.2ml is+/- 0.07ml
Sterilization Method	EO, Radiation
Not made with BPA	BPA Free
DEHP Free	Not made with DEHP
Latex Statement	Not made with natural rubber latex
PVC Free	Not made with PVC
Disposable	Disposable product
Single Use	Product is for single use only

Regulatory Compliance and Quality System

BD Products comply with the regulatory requirements of the region in which these are sold and manufactured.

Sterility

All products which are labeled as #sterile# and released for sale by BD are certified to be sterile as long as the package is unopened and undamaged. For those products labeled #sterile fluid path#, only the fluid path is sterile.

This product is primarily sterilized via E-beam. Sterilization cycle development/validation is performed to 10^-6SAL in accordance with current ISO 11137 guidelines.

Pyrogenicity

All products which are labeled as non-pyrogenic and released for sale by BD have been tested per United States Pharmacopeia (USP) chapter 85 – Bacterial Endotoxins Test and meets limits as specified in chapter 161- Transfusion and Infusion Assemblies and Similar Medical Devices.

Quality Control Testing and Release

Representative production samples are collected and inspected in accordance with current applicable product specifications. Inspection records are reviewed and signed off by qualified personnel for product release. The released devices meet applicable BD product specifications.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)	No
Device labeled as “Not made with natural rubber latex”	No
For Single-Use	Yes
Prescription Use (Rx)	Yes
Over the Counter (OTC)	No
Kit	No
Combination Product	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)	No