FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: 10304040154233 · Model: 5702709 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Henry Schein
Primary DI
10304040154233
Version / Model
5702709
Catalog Number
5702709
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2021-06-24
Public Version
1
Public Version Date
2021-07-02
Public Version Status
New
Public Device Record Key
175541d7-78f1-49b8-aee9-7453e7582b00

Device Description

Needle Disposable Safety 30Gx1/2

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
Yes

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FMI Needle, hypodermic, single lumen

GMDN Terms

Code Name
59232 Mobile orthovoltage therapeutic x-ray system

Identifiers

Type ID
Package 20304040154230
Primary 10304040154233
Unit of Use 00304040154236