KangLi Pedicle Screw Spinal System

FDA UDI

Class II (US FDA UDI)

by Suzhou Kangli Orthopaedics Instrument Co., Ltd.

Identity

Trade Name: KangLi Pedicle Screw Spinal System FDA UDI
Generic Name: Bone-screw internal spinal fixation system rod FDA UDI
Device Name: Rod (φ6.0) FDA UDI
Model / Reference: T6160040 FDA UDI
Description: Rod (φ6.0) FDA UDI

Identifiers

Catalog Number: T6160040 FDA UDI
Primary DI / UDI-DI: 06937762187325 FDA UDI
510(k) Number: K142290 FDA UDI
FDA Product Code: MNH FDA UDI
MNI FDA UDI
GMDN Term: Bone-screw internal spinal fixation system rod FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3070 FDA UDI
Commercial Distribution: Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 40 Millimeter FDA UDI

KangLi Pedicle Screw Spinal System by Suzhou Kangli Orthopaedics Instrument Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Suzhou Kangli Orthopaedics Instrument Co., Ltd.

Sources (1)

FDA UDI 65c511b6-2e22-4a86-8a15-8ada18590895 37 fields · synced Jun 1, 2026