AccessGUDID - DEVICE: BD Blunt Filter NRFit (00382904000660)

GUDID

Device Identifier (DI) Information

Brand Name: BD Blunt Filter NRFit
Version or Model: 400066
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 400066
Company Name: BECTON, DICKINSON AND COMPANY

Primary DI Number: 00382904000660
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 001292192 *Terms of Use

Device Description: BD® Blunt Filter NRFit™ Needle, 18G x 1 1/2 in

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

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
16627	Medication transfer needle, non-filtering/non-vented	A slender, rigid, sharp or blunt metal tube intended to be attached to a syringe and typically used in the pharmacy to aspirate and transfer fluid medication from a vial/ampule to another container for medication preparation or other purposes. It consists of a short needle sufficient to penetrate the vial stopper and extract all the medication. It is typically of 20 gauge to provide a high-flow rate with minimum coring. It does not include a filter or a back-pressure venting feature. This is a single-use device.	Active	false
64357	Medication transfer straw	A slender flexible tube with a blunt distal end intended to be attached to a syringe to aspirate pharmaceutical fluids from an open vial or ampule during the preparation of medications performed by healthcare professionals (e.g., pharmacists, physicians, nurses); it is not intended to puncture the seal of a vial/container. It is typically made of plastic and may include an integral filter intended to retain micro-particles to reduce the risk of particle contamination of the patient medication. It is not intended for skin injections or tissue manipulation and is not intended for enteral use. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GAA	NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE

FDA Premarket Submission

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

Device Exempt from Premarket Submission: Yes 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: Keep dry
Special Storage Condition, Specify: Fragile, handle with care
Special Storage Condition, Specify: Keep away from sunlight
Special Storage Condition, Specify: Room Temperature

Clinically Relevant Size

[?]

Size Type Text
Length: 40 Millimeter
Needle Gauge: 18 Gauge

Device Record Status

Public Device Record Key: 049023c2-9c76-4c7a-b7df-ce48b3733f6b
Public Version Date: July 17, 2025
Public Version Number: 2
DI Record Publish Date: August 01, 2022