FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: 00304040128633 · Model: 1007730 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Henry Schein
Primary DI
00304040128633
Version / Model
1007730
Catalog Number
1007730
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-06
Public Version
2
Public Version Date
2020-08-05
Public Version Status
Update
Public Device Record Key
4bbc19b9-70b7-424d-aa53-0175b91cc8dc

Device Description

Curette Bone DE Lucas

Device Characteristics

Single Use
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
EKE CURETTE, OPERATIVE

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 00304040128633