FDA UDI In Commercial Distribution 🇺🇸 United States

Kyocera Medical Technologies, Inc.

DI: 00841523137336 · Model: S 128 · KYOCERA MEDICAL TECHNOLOGIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kyocera Medical Technologies, Inc.
Primary DI
00841523137336
Version / Model
S 128
Catalog Number
2130-423-219
Company Name
KYOCERA MEDICAL TECHNOLOGIES, INC.
Labeler DUNS
116995646
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-17
Public Version
3
Public Version Date
2019-03-27
Public Version Status
Update
Public Device Record Key
d25aef3f-6165-4fea-932b-4a49f2f4db75

Device Description

Broach, 42 X 32, 19mm Height 7° Lordosis

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
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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00841523137336