AccessGUDID - DEVICE: BD Neoflon Pro Safety Safety IV Catheter (00382903916603)

GUDID

Device Identifier (DI) Information

Brand Name: BD Neoflon Pro Safety Safety IV Catheter
Version or Model: 391660
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 391660
Company Name: BECTON, DICKINSON AND COMPANY

Primary DI Number: 00382903916603
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 124987988 *Terms of Use

Device Description: NEOFLON PRO SAFETY 24GX0.75IN STRAIGHT

Device Characteristics

What MRI safety information does the labeling contain?	MR Conditional
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":	Yes
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

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
64574	Peripheral intravenous cannula	A short, thin tube intended to be inserted into a peripheral vein (typically on the hand/arm) to enable short-term (< 30 days) intravenous (IV) access for administration of fluids/medication and blood sampling. Also referred to as a peripheral IV catheter, it is typically assembled with a dedicated introduction needle, and usually includes connectors, injection ports, and wings for fixation. It is not intended to be advanced to the central vasculature. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FOZ	Catheter, intravascular, therapeutic, short-term less than 30 days

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: Fragile, handle with care
Special Storage Condition, Specify: Keep away from sunlight
Special Storage Condition, Specify: Keep dry

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: Size = Catheter Gauge = 24 Gauge (G)
Device Size Text, specify: Flow Rate = 20 millilitre per minute (mL or ml/min)
Length: 19 Millimeter

Device Record Status

Public Device Record Key: 530a32e6-8f7a-4f22-9d45-2afe4b7d7f87
Public Version Date: July 29, 2025
Public Version Number: 3
DI Record Publish Date: October 22, 2018