FDA UDI In Commercial Distribution 🇺🇸 United States

Medtronic Resuable Instruments

DI: 00643169782709 · Model: X0516051 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medtronic Resuable Instruments
Primary DI
00643169782709
Version / Model
X0516051
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-08
Public Version
1
Public Version Date
2022-09-16
Public Version Status
New
Public Device Record Key
4e0b6b5b-8d39-457b-929f-1aa36a0ae80e

Device Description

CURETTE X0516051 STRAIGHT SHAFT 1.8MM

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
Yes
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
FZS CURETTE, SURGICAL, GENERAL USE

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 00643169782709

Customer Contacts