FDA UDI In Commercial Distribution 🇺🇸 United States

Medtronic Reusable Instrument

DI: 20763000211015 · Model: 6550102 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

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Basic Information

Brand Name
Medtronic Reusable Instrument
Primary DI
20763000211015
Version / Model
6550102
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2022-10-16
Public Version
1
Public Version Date
2022-10-24
Public Version Status
New
Public Device Record Key
9bc0b226-6852-46c1-9ecf-cce00ab6e7b3

Device Description

BONE FILLER DEVICE 6550102 BOX OF 2 BFD

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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KIH DISPENSER, CEMENT

GMDN Terms

Code Name
35809 Orthopaedic cement dispenser

Identifiers

Type ID
Unit of Use 00763000211011
Primary 20763000211015

Customer Contacts