FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: 00304040017050 · Model: 9007640 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Henry Schein
Primary DI
00304040017050
Version / Model
9007640
Catalog Number
9007640
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
3
Public Version Date
2018-09-12
Public Version Status
Update
Public Device Record Key
20e3c31e-ad95-41b6-a9a1-4195f94e7a01

Device Description

Syringe/Needle Combo Safety3cc

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
FMF Syringe, piston

GMDN Terms

Code Name
47017 General-purpose syringe, single-use

Identifiers

Type ID
Package 10304040017057
Primary 00304040017050
Unit of Use 20304040017054