DEVICE: KMC Balloon Catheter, 10 Gauge, 15mm (06938695546203)
Device Identifier (DI) Information
KMC Balloon Catheter, 10 Gauge, 15mm
KMC-004-15
In Commercial Distribution
Shanghai Kinetic Medical Co., Ltd.
KMC-004-15
In Commercial Distribution
Shanghai Kinetic Medical Co., Ltd.
KMC Balloon Catheter, 10 Gauge, 15mm
Device Characteristics
| Labeling does not contain MRI Safety Information | |
| No | |
| No | |
| Yes | |
| Yes | |
| No | |
| No | |
| No | |
| No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
| GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
|---|---|---|---|---|
| 47021 | Inflatable bone tamp |
A catheter-like device with an inflatable balloon at the distal end used for the reduction of fractures and/or creation of a void in cancellous bone [e.g., in the spine for a vertebral compression fracture (VCF), hand, tibia, radius, and calcaneus]. It is commonly used for kyphoplasty, which involves its insertion into a patient's back to reduce a vertebral body fracture by compression of cancellous bone and/or movement of the endplates as the balloon is inflated. After the device is removed, orthopaedic bone cement is introduced into the created void to stabilize the vertebra. This is a single-use device.
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Active | false |
FDA Product Code
[?]| Product Code | Product Code Name |
|---|---|
| NDN | Cement, Bone, Vertebroplasty |
| HRX | Arthroscope |
FDA Premarket Submission
| FDA Premarket Submission Number [?] | Supplement Number [?] |
|---|---|
| K113742 | 000 |
Sterilization
Storage and Handling
[?]| Storage and Handling |
|---|
| Storage Environment Humidity: less than 80 Percent (%) Relative Humidity |
| Storage Environment Temperature: between 18 and 25 Degrees Celsius |
Clinically Relevant Size
[?]| Size Type Text |
|---|
| Balloon Length: 15 Millimeter |
Device Record Status
097306bf-ccab-43be-8be6-6e1939cf9b4b
October 09, 2020
1
October 01, 2020
October 09, 2020
1
October 01, 2020
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]| Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
|---|---|---|---|---|---|
| No Package DIs found | |||||
Secondary DI
[?]| Issuing Agency [?] | Secondary DI Number |
|---|---|
| No Secondary DIs found | |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+862150720558
qingmeiwei@shkmc.com.cn
qingmeiwei@shkmc.com.cn