FDA UDI In Commercial Distribution 🇺🇸 United States

KYPHON Express KyphoPak Tray

DI: 00763000031800 · Model: KPE1001 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KYPHON Express KyphoPak Tray
Primary DI
00763000031800
Version / Model
KPE1001
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-26
Public Version
1
Public Version Date
2019-02-26
Public Version Status
New
Public Device Record Key
ef1a2adc-d66b-46f0-9be9-553d5cf5258a

Device Description

KIT KPE1001 KYPAK EXP TRY 10/2 FF W/EOIS

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
No
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
HRX Arthroscope

GMDN Terms

Code Name
47129 Balloon kyphoplasty kit

Identifiers

Type ID
Primary 00763000031800

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K041454 000

Storage Conditions

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