Kyphoplasty Balloon Catheter

Primary DI
06923558509709
Brand
Kyphoplasty Balloon Catheter
Company
Jiangsu Changmei Medtech Co., Ltd.
Model
KB0210S1
Device description
cylindrical type, balloon size 10mm, working channel greater than or equal to 3.1mm, with needle-free connector
Published
2025-10-21
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HRXArthroscope
HXGTamp

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HRXArthroscopeOrthopedic2
HXGTampOrthopedic1

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K223709000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K223709000Kyphoplasty Balloon CatheterJiangsu Changmei Medtech Co., Ltd.2023-08-16HRX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
06923558509709PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
06923558509709069235585097096923558509709

GMDN Terms#

Term, Definition table
TermDefinition
Kyphoplasty balloon catheterA sterile, flexible tube designed to be used for the creation of a void within a vertebral body during a minimally invasive procedure commonly known as balloon kyphoplasty. It is manually inserted percutaneously through an access channel under fluoroscopic guidance to a vertebral compression fracture (VCF) site (e.g., in the lumbar or thoracic region of the spine) where its balloon is inflated with a medium (e.g., a liquid contrast medium) to force the vertebrae apart for insertion of bone cement; thereafter it is deflated and removed via the access channel. This is a single-use device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Storage Environment Humidity0 Percent (%) Relative Humidity80 Percent (%) Relative Humidity

Contacts#

Phone, Email table
PhoneEmail
+008651988520118sales@czmed.com

Regulatory Flags#

DUNS number
560432633
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
06923558507569Kyphoplasty Tool KitKT-00-052025-10-23
06923558509693Kyphoplasty Tool KitKT-00-062025-10-23
06923558506487Balloon InflatorBI-20A-102025-10-21
06923558506968Kyphoplasty Balloon CatheterKB0120S12025-10-21
06923558507385Kyphoplasty Balloon CatheterKB0115S12025-10-21

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