FDA UDI In Commercial Distribution 🇺🇸 United States

KYPHON® Inflation Syringe

DI: 00643169097155 · Model: A08E · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
KYPHON® Inflation Syringe
Primary DI
00643169097155
Version / Model
A08E
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-02
Public Version
5
Public Version Date
2020-05-06
Public Version Status
Update
Public Device Record Key
025d8bae-5bbd-40c0-bb0e-84dee7786df4

Device Description

SYRINGE A08E KIS INFLATION HP

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
HXG TAMP

GMDN Terms

Code Name
17541 Catheter/overtube balloon inflator, single-use

Identifiers

Type ID
Primary 00643169097155

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K103231 000