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BD 305200 - NEEDLE FILTER 15 19 GAUGE 1000/CS

BD  # 305200 - NEEDLE FILTER 15 19 GAUGE 1000/CS
Part Number BD 305200
SKU Number CIA3017964
Sell Unit CASE
Ships Within Special Order
List Price $311.28
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Product Description

BD 305200 - NEEDLE FILTER 15 19 GAUGE 1000/CS

305200 - 19 G BD 5 Micron Filter Needle 1 1/2 In., Sterile, Single Use with 5-Micron Filter Membrane

5 Micron Filter Stops 98% of Particulates

BD filter needles feature a molded-in 5-micron filter membrane that reduces larger particles during fluid aspiration, reconstitution or transfer, and during medication withdraw from glass reservoirs. 5 micron filter mem-brane that is designed to prevent large particles being drawn into the syringe when preparing medications from ampules.


Key Product Features

CE MarkProduct is CE-marked
Hub ColorClear
Hub MaterialPolycarbonate
Hub TypeLuer
Needle Gauge19 G
Needle Gauge (m)1.10 mm
Needle Length (in.)1 1/2 in.
Needle Length (m)38.10 mm
Needle Wall TypeRegular
Needle TypeFilter
Needle Wall TypeRegular
Total Shelf Life1825
SterileSterilized product
Type Of BevelRegular
Sterilization MethodRadiation
DEHP FreeNot made with DEHP
Latex StatementNot made with natural rubber latex
PVC FreeNot made with PVC
DisposableDisposable product
Single UseProduct 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 ETO. Sterilization cycle development/validation is performed to 10-6 SAL 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.

Biocompatability

This product has been evaluated in accordance with ISO 10993 "Biological Evaluation of Medical Devices", and complies with all relevant sections.

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-UseYes
Prescription Use (Rx)No
Over the Counter (OTC)No
KitNo
Combination ProductNo
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)No

Product Packaging Information

Packaging LevelShelfpackEachCase
Quantity10011000
Length115.0 mm449.58 mm
Width86.0 mm203.2 mm
Height96.0 mm129.54 mm
Weight186.0 g1.86 g1.86 kg
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