FDA UDI In Commercial Distribution 🇺🇸 United States

Kyphoplasty Tool Kit

DI: 06923558507569 · Model: KT-00-05 · Jiangsu Changmei Medtech Co., Ltd.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kyphoplasty Tool Kit
Primary DI
06923558507569
Version / Model
KT-00-05
Company Name
Jiangsu Changmei Medtech Co., Ltd.
Labeler DUNS
560432633
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-23
Public Version
1
Public Version Date
2025-10-31
Public Version Status
New
Public Device Record Key
62e8b7b2-bc3d-4dc4-b0ed-8aa439f29ee2

Device Description

Kyphoplasty Tool Kit (Bilateral standard type)

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OCJ Spinal Channeling Instrument, Vertebroplasty
OAR Injector, Vertebroplasty (Does Not Contain Cement)
KIH Dispenser, Cement
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
58031 Bone access channel kit

Identifiers

Type ID
Primary 06923558507569

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
– 80 Percent (%) Relative Humidity