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KangLi Pedicle Screw Spinal System
FDA UDIEUDAMEDClass II (US FDA UDI)
Ref T5816550Model Non-sterile Spinal Systems(KSS-II, III Lumbar)
Identity
- Trade Name
- KangLi EUDAMEDKangLi Pedicle Screw Spinal System FDA UDI
- Generic Name
- Spinal bone screw, non-bioabsorbable FDA UDI
- Device Name
- Non-sterile Spinal Systems EUDAMEDKSS 6.0 U-Pedicle Screw φ6.5×50mm FDA UDI
- Model / Reference
- T5816550 EUDAMEDFDA UDINon-sterile Spinal Systems(KSS-II, III Lumbar) EUDAMED
- Description
- KSS 6.0 U-Pedicle Screw φ6.5×50mm FDA UDI
Identifiers
- Catalog Number
- T5816550 FDA UDI
- Primary DI / UDI-DI
- 06937762171423 EUDAMEDFDA UDI
- Basic UDI-DI
- 690295900030FD EUDAMED
- Direct Marketing DI
- 06937762171423 EUDAMED
- 510(k) Number
- K142290 FDA UDI
- FDA Product Code
- MNH FDA UDIMNI FDA UDI
- EMDN Code
- P09070302 THORACOLUMBOSACRAL FIXATION SYSTEMS EUDAMED
- GMDN Term
- Spinal bone screw, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 888.3070 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
Yes
EUDAMED
Sutures
Yes
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 50 Millimeter FDA UDI
KangLi Pedicle Screw Spinal System by Suzhou Kangli Orthopaedics Instrument Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID, EUDAMED
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 (2)
- FDA UDI 17d1fd1a-a0f1-45d4-b472-8ac49b09d1f4 37 fields · synced Oct 7, 2026
- EUDAMED f8bfd323-5631-46eb-b0af-a0bfdf0ca252 61 fields · synced Jul 15, 2026