FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00382904050108 · Model: 405010 · BECTON, DICKINSON AND COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
N/A
Primary DI
00382904050108
Version / Model
405010
Catalog Number
405010
Company Name
BECTON, DICKINSON AND COMPANY
Labeler DUNS
001292192
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
5
Public Version Date
2025-07-04
Public Version Status
Update
Public Device Record Key
43dad772-bfc8-4a5e-b76f-da3089b6c31f

Device Description

NEEDLE SPINAL S/SU 22GA 3-1/2IN WHITACRE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

GMDN Terms

Code Name
35212 Spinal needle, single-use

Identifiers

Type ID
Package 50382904050103
Primary 00382904050108
Package 30382904050109

Device Sizes

Type Value Unit Text
Length 3.5 Inch
Needle Gauge 22 Gauge