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KMC Biopsy Device, 8 Gauge, Square Tip

FDA UDI

Class II (US FDA UDI)

by Shanghai Kinetic Medical Co., Ltd.

Identity

Trade Name
KMC Biopsy Device, 8 Gauge, Square Tip FDA UDI
Generic Name
Balloon kyphoplasty kit FDA UDI
Device Name
KMC Biopsy Device, 8 Gauge, Square Tip FDA UDI
Model / Reference
KMC-015-10 FDA UDI
Description
KMC Biopsy Device, 8 Gauge, Square Tip FDA UDI

Identifiers

Primary DI / UDI-DI
06938695546425 FDA UDI
510(k) Number
K113742 FDA UDI
FDA Product Code
NDN FDA UDI
HRX FDA UDI
GMDN Term
Balloon kyphoplasty kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3027 FDA UDI
888.1100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 8 Gauge FDA UDI

Category: Balloon kyphoplasty kit

A comprehensive medical device directory, featuring the KMC Biopsy Device, a high-quality 8 Gauge, square tip biopsy tool used in orthopedic procedures.

Similar devices

Also classified as Balloon kyphoplasty kit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 43ddabef-83eb-41bc-adc2-77dc83b210de 37 fields · synced Aug 3, 2026