FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: 00304040057056 · Model: 5700618 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Henry Schein
Primary DI
00304040057056
Version / Model
5700618
Catalog Number
5700618
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-17
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
fdb76238-8062-4d01-a0d9-daf8fe1e046c

Device Description

Suture Removal Kit with PVP

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
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
KKX Drape, surgical

GMDN Terms

Code Name
13894 Suture removal kit

Identifiers

Type ID
Package 10304040057053
Primary 00304040057056