FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: 10304040025946 · Model: 5700342 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Henry Schein
Primary DI
10304040025946
Version / Model
5700342
Catalog Number
5700342
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2019-10-23
Public Version Status
Update
Public Device Record Key
2c470e5f-67dc-436a-9e7f-03e0f2261aef

Device Description

Needle Disposable Safety

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
FMI Needle, hypodermic, single lumen

GMDN Terms

Code Name
59230 Hypodermic needle, single-use

Identifiers

Type ID
Package 20304040025943
Primary 10304040025946
Unit of Use 00304040025949