FDA UDI In Commercial Distribution 🇺🇸 United States

KYPHON® Bone Biopsy Device

DI: 00763000311674 · Model: F05A · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KYPHON® Bone Biopsy Device
Primary DI
00763000311674
Version / Model
F05A
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-06
Public Version
1
Public Version Date
2020-11-16
Public Version Status
New
Public Device Record Key
0d9dfbcd-d00d-481b-acdb-e47cf7a1b1df

Device Description

BONE BIOPSY DEVICE F05A SIZE 3-RB

Device Characteristics

Single Use
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KIH DISPENSER, CEMENT

GMDN Terms

Code Name
60478 Bone access cannula

Identifiers

Type ID
Primary 00763000311674

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool, dry place